Basic information Safety Supplier Related

(R)-1-Boc-3-cyanopyrrolidine

Basic information Safety Supplier Related

(R)-1-Boc-3-cyanopyrrolidine Basic information

Product Name:
(R)-1-Boc-3-cyanopyrrolidine
Synonyms:
  • (R)-1-Boc-3-cyanopyrrolidine
  • (R)-1-Boc-3-cyanopyrrolid...
  • tert-butyl (3R)-3-cyanopyrrolidine-1-carboxylate
  • (R)-N-Boc-Cyanopyrrolidine
  • (R)-1-N-Boc-3-Cyano-pyrrolidine(R)-1-N-Boc-3-Cyano-pyrrolidine
  • (R)-1-Boc-3-cyanopyrrolidine 95+%
  • 1-Pyrrolidinecarboxylic acid, 3-cyano-, 1,1-dimethylethyl ester, (3R)-
  • tert-butyl (R)-3-cyanopyrrolidine-1-carboxylate
CAS:
132945-76-7
MF:
C10H16N2O2
MW:
196.25
Product Categories:
  • Pyrrole&Pyrrolidine&Pyrroline
Mol File:
132945-76-7.mol
More
Less

(R)-1-Boc-3-cyanopyrrolidine Chemical Properties

Boiling point:
307.9±35.0 °C(Predicted)
Density 
1.08±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
form 
solid
pka
-3.73±0.40(Predicted)
Appearance
white solid
optical activity
[α]/D -21.0±2.0°, c = 1 in methanol
BRN 
8683216
CAS DataBase Reference
132945-76-7(CAS DataBase Reference)
More
Less

Safety Information

Hazard Codes 
Xn
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HS Code 
2933998090
More
Less

(R)-1-Boc-3-cyanopyrrolidine Usage And Synthesis

Uses

(R)-1-Boc-3-cyanopyrrolidine can be used as a key intermediate in the synthesis of a β-proline analog named (3R)-carboxy pyrrolidine.

Uses

(R)-1-Boc-3-cyanopyrrolidine is used in the preparation of 1-Azabicyclo[3.2.0]hept-2-ene-2-carboxylic Acid compounds as anti-microbial agents.

Synthesis

773837-37-9

132945-75-6

132945-76-7

The general procedure for the synthesis of (R)-1-Boc-3-cyanopyrrolidine from the compound (CAS: 773837-37-9) and S-1-Boc-3-OMS-pyrrolidine is as follows: b) Synthesis of 1,1-dimethylethyl (3R)-3-cyano-1-pyrrolidine carboxylate A mixture of 1,1-dimethylethyl (3S)-3-[(methylsulfonyl)oxy]-1-pyrrolidine carboxylic acid ester (211 mmol) with sodium cyanide (633 mmol) in N,N-dimethylformamide (300 mL) was stirred vigorously for 18 h at 100 °C in a nitrogen atmosphere using a mechanical stirrer. After completion of the reaction, the mixture was cooled to room temperature, filtered and washed well with ether. The filtrate was diluted with dilute brine and extracted with ether (4 x 700 mL). The organic extracts were combined, washed with dilute brine, filtered through a pad of sodium sulfate and subsequently concentrated under vacuum. The residue was purified by fast chromatography (eluent: 0-50% ethyl acetate/hexane) to afford the target product (141 mmol, 67% yield). 1H NMR (400 MHz, CDCl3) δ ppm: 1.48 (s, 9H), 2.14-2.37 (m, 2H), 3.00-3.20 (m, 1H), 3.45 (dt, J = 11.05, 6.98 Hz, 1H), 3.53-3.66 (m, 2H), 3.65-3.76 (m, 1H).

References

[1] Patent: WO2011/56635, 2011, A1. Location in patent: Page/Page column 49-50
[2] Patent: WO2011/66211, 2011, A1. Location in patent: Page/Page column 35
[3] Patent: WO2013/28445, 2013, A1. Location in patent: Page/Page column 51
[4] Patent: WO2012/37298, 2012, A1. Location in patent: Page/Page column 82

(R)-1-Boc-3-cyanopyrrolidineSupplier

J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com
Chembest Research Laboratories Limited
Tel
+86-21-20908456
Email
sales@BioChemBest.com
Alfa Aesar
Tel
400-6106006
Email
saleschina@alfa-asia.com
Energy Chemical
Tel
021-021-58432009 400-005-6266
Email
sales8178@energy-chemical.com
Capot Chemical Co., Ltd
Tel
+86 (0) 571 85 58 67 18