| Identification | More | [Name]
(R)-1-Boc-3-cyanopyrrolidine | [CAS]
132945-76-7 | [Synonyms]
(R)-1-Boc-3-cyanopyrrolidine | [Molecular Formula]
C10H16N2O2 | [MDL Number]
MFCD05863904 | [Molecular Weight]
196.25 | [MOL File]
132945-76-7.mol |
| Hazard Information | Back Directory | [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. | [Synthesis]
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 |
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