N-Boc-2-piperidone

  • Name: N-Boc-2-piperidone
  • CAS: 85908-96-9
  • Purity: 99%
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1.What is the N-Boc-2-piperidone ?

Intermediate in the preparation of various biological inhibitors.

piperidin-2-one
675-20-7

piperidin-2-one

di-<i>tert</i>-butyl dicarbonate
24424-99-5

di-tert -butyl dicarbonate

2-oxopiperidine-1-carboxylic acid tert-butyl ester
85908-96-9

2-oxopiperidine-1-carboxylic acid tert-butyl ester

Conditions
Conditions Yield
piperidin-2-one; With n-butyllithium; In tetrahydrofuran; at -78 ℃; for 0.166667h;
di-tert-butyl dicarbonate; In tetrahydrofuran; at -78 ℃; for 0.5h; Further stages.;
99%
piperidin-2-one; With n-butyllithium; In tetrahydrofuran; at -78 ℃; for 0.5h; Inert atmosphere;
di-tert-butyl dicarbonate; In tetrahydrofuran; at 20 ℃; for 16h; Inert atmosphere;
98%
piperidin-2-one; With n-butyllithium; In tetrahydrofuran; hexane; at -78 ℃; for 0.166667h; Inert atmosphere;
di-tert-butyl dicarbonate; In tetrahydrofuran; hexane; at -78 ℃; for 0.75h; Inert atmosphere;
97%
With dmap; In acetonitrile; at 20 ℃; for 1h;
96%
With dmap; triethylamine; In dichloromethane; at 20 ℃; for 3h;
91%
With dmap; triethylamine; In dichloromethane; at 20 ℃; for 3h;
91%
With dmap; triethylamine; In dichloromethane; at 20 ℃; for 3h;
91%
With dmap; triethylamine; In dichloromethane; at 20 ℃; for 3h;
91%
With n-butyllithium; In dichloromethane; at -78 - 20 ℃;
90%
With dmap; In acetonitrile; at 20 ℃; for 5h;
90%
With dmap; In acetonitrile; at 20 ℃;
88%
With dmap; In tetrahydrofuran; at 20 ℃; for 18h; Inert atmosphere;
86%
With dmap; In dichloromethane;
85%
With dmap; triethylamine; In dichloromethane; at 0 - 20 ℃; for 48h;
85%
With dmap; triethylamine; In dichloromethane; at 0 - 20 ℃; for 48h;
85%
With dmap; triethylamine; In dichloromethane; at 25 ℃; for 8h;
84%
With dmap; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; Inert atmosphere;
84%
With dmap; In acetonitrile; at 20 ℃; for 2h;
83%
With dmap; In acetonitrile; at 22 ℃; for 2h; Reagent/catalyst; Solvent; Temperature;
82%
With triethylamine; dmap; In dichloromethane; at 20 ℃; for 32h;
81%
With dmap; triethylamine; In dichloromethane; at 0 - 20 ℃; Inert atmosphere;
81%
With dmap; triethylamine; In dichloromethane; at 0 - 20 ℃;
80%
With dmap; triethylamine; In dichloromethane; at 25 ℃; for 8h; Inert atmosphere;
80%
dmap; In acetonitrile;
79%
piperidin-2-one; With n-butyllithium; In tetrahydrofuran; at -78 ℃; for 0.25h;
di-tert-butyl dicarbonate; In tetrahydrofuran; at -78 - 20 ℃; Further stages.;
78%
With dmap; triethylamine; In acetonitrile; at 0 - 20 ℃; for 18h;
77%
With dmap; In acetonitrile; for 24h; Ambient temperature;
74%
With dmap; triethylamine; In dichloromethane; at 20 ℃; for 12h;
74%
piperidin-2-one; With n-butyllithium; In tetrahydrofuran; at -78 ℃; for 0.25h; Inert atmosphere;
di-tert-butyl dicarbonate; In tetrahydrofuran; at -78 ℃; for 0.5h; Inert atmosphere;
72%
With dmap; triethylamine; In dichloromethane; at 0 - 20 ℃; for 12h;
68%
With dmap; triethylamine; In acetonitrile; at 18 ℃; for 16h; Inert atmosphere;
67.25%
With dmap; triethylamine; In dichloromethane; at 25 ℃; for 16h;
50%
With dmap; In dichloromethane; at 20 ℃; for 24h;
48%
With n-butyllithium; Yield given. Multistep reaction; 1.) THF, -78 deg C, 30 min, 2.) 3 h;
With dmap; In acetonitrile; for 4h; Ambient temperature;
0.90 g
With n-butyllithium; Multistep reaction; 1) THF, -78 deg C, 30 min; 2) THF, -78 deg C, 3 h;
With dmap; In dichloromethane;
With dmap; triethylamine; In hexane; dichloromethane; ethyl acetate;
piperidin-2-one; With lithium diisopropyl amide; In tetrahydrofuran; at -70 - -60 ℃; for 1h;
di-tert-butyl dicarbonate; In tetrahydrofuran; at -70 - 20 ℃;
With water; In tetrahydrofuran; toluene; for 0.5h;
piperidin-2-one; With n-butyllithium; In tetrahydrofuran; hexane; at 0 ℃; for 1h; Inert atmosphere;
di-tert-butyl dicarbonate; In tetrahydrofuran; hexane; at 0 ℃; for 2h; Inert atmosphere;
piperidin-2-one; With dmap; triethylamine; In acetonitrile; at 0 ℃; for 0.166667h;
di-tert-butyl dicarbonate; In acetonitrile; at 20 ℃; for 2h;
With dmap; In acetonitrile; at 0 ℃; for 24h;
6.07 g
With dmap; In acetonitrile; at 20 ℃; for 3h; Inert atmosphere;
With dmap; triethylamine; In dichloromethane;
With dmap; triethylamine; In dichloromethane; at 20 ℃; for 3h;
With dmap; TEA; In dichloromethane; at 0 - 20 ℃;
piperidin-2-one; With n-butyllithium; In tetrahydrofuran; hexane; at 0 ℃; for 0.5h; Inert atmosphere;
di-tert-butyl dicarbonate; In tetrahydrofuran; water; at 0 - 20 ℃; for 2h; Inert atmosphere;
With dmap; triethylamine; In dichloromethane; at 20 ℃; for 24h;
piperidone monohydrate hydrochloride

piperidone monohydrate hydrochloride

di-<i>tert</i>-butyl dicarbonate
24424-99-5

di-tert -butyl dicarbonate

2-oxopiperidine-1-carboxylic acid tert-butyl ester
85908-96-9

2-oxopiperidine-1-carboxylic acid tert-butyl ester

Conditions
Conditions Yield
With potassium hydrogensulfate; N-ethyl-N,N-diisopropylamine; In methanol;
93%

2.What is the CAS number for N-Boc-2-piperidone ?

The CAS number of N-Boc-2-piperidone is 85908-96-9.

More information of N-Boc-2-piperidone 85908-96-9 are:

CAS?Number

85908-96-9

Density

1.099 g/cm3

Melting Point

34-37 °C

Boiling Point

319.7 °C at 760 mmHg

Flash Point

147.1 °C

Vapor Pressure

0.000334mmHg at 25°C

Refractive Index

1.481

HS CODE

29337900

PSA

46.61000

LogP

1.87190

Pka

-2.29±0.20(Predicted)

3.What are another words for N-Boc-2-piperidone ?

Synonyms?for?N-Boc-2-piperidone 85908-96-9:1,1-Dimethylethyl2-oxopiperidine-1-carboxylate;2-Oxopiperidine-1-carboxylic acid tert-butylester;N-tert-Butoxycarbonyl-2-piperidinone;tert-Butyl2-oxopiperidine-1-carboxylate;

4.What is the molecular formula of N-Boc-2-piperidone?

The chemical formula of ?N-Boc-2-piperidone is?C10H17NO3 which containing 10 Carbon atoms,17 Hydrogen atoms,1 Nitrogen atoms and 3 Oxygen atoms,and the molecular weight of??N-Boc-2-piperidone?is 199.25.

5.What is N-Boc-2-piperidone (85908-96-9) used for?

InChI:InChI=1/C10H17NO3/c1-10(2,3)14-9(13)11-7-5-4-6-8(11)12/h4-7H2,1-3H3

Relevant articles related to N-Boc-2-piperidone:

Article

Source

TMSOTf-mediated approach to 1,3-oxazin-2-one skeleton through one-pot successive reduction-[4 + 2] cyclization process of imides with ynamides

Zhang, Chen-Chen,Huo, Zhi-Peng,Tang, Mei-Lin,Liang, Yong-Xi,Sun, Xun

supporting information, (2021/03/15)

Br?nsted Acid-Catalyzed Aza-Ferrier Reaction of N, O-Allenyl Acetals: Synthesis of β-Amino-α-methylene Aldehydes

Tayama, Eiji,Ishikawa, Yuki

supporting information, p. 9405 - 9414 (2020/08/14)

6.Buy N-Boc-2-piperidone with the best price .

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