Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457201Generated: October 29, 2026

Acetic Acid → 3-[(4-Chloro-benzyl)-methoxycarbonylmethyl-amino]-pyrrolidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/457201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-ChlorobenzaldehydeHCID 7726—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantTert-butyl 3-[(2-methoxy-2-oxoethyl)amino]pyrrolidine-1-carboxylateHCID 66758491—
Solvent1,1-DichloroethaneHCID 6365—
Product3-[(4-Chloro-benzyl)-methoxycarbonylmethyl-amino]-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 66758384—

Reaction Steps

To a solution of 3-(methoxycarbonylmethyl-amino)-pyrrolidine-1-carboxylic acid tert-butyl ester (0.5 g, 2.03 mmol) in dichloroethane (5.0 mL) was added 4-chlorobenzaldehyde (0.34 g, 2.44 mmol), sodium triacetoxy borohydride (0.86 g, 4.06 mmol) and catalytic acetic acid and the resulting mixture was stirred at room temperature overnight. The reaction mixture was concentrated, dissolved in dichloromethane and washed with 10% aqueous sodium bicarbonate. The combined organics were washed with brine and dried over sodium sulfate. The crude product was purified on silica using ethyl acetate. 1H-NMR (CDCl3) δ: 1.40 (9H, s), 1.80 (1H, m), 2.10 (1H, m), 3.00–3.80 (7H, m), 4.70(1H, br,s), 7.20 (4H,m). ESI-MS m/z: 383(M+1), UV retention time: 2.91 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07186729B2
Source datasetuspto-grants-2007_03
ORD IDord-5924aec1a2014aa395511186f0fe9c07
Source noteuspto-grants-2007_03