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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242674Generated: October 31, 2026

Acetic Acid → HCID 66758387, compound

https://huagongshe.com/reaction/242674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant4-ChlorobenzaldehydeHCID 7726—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant3-(Carbamoylmethyl-amino)-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 66758446—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 66758387HCID 66758387—

Reaction Steps

To a solution of 3-(carbamoylmethyl-amino)-pyrrolidine-1-carboxylic acid tert-butyl ester (0.49 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: 1.50 (9H, s), 1.60-1.80 (2H, m), 2.10 (1H, m), 3.10-3.60 (8H, m), 5.65 (1H, br, s), 6.90 (1H, br, s) 7.20-7.40 (4H, m). ESI-MS m/z: 367(M+1), UV retention time: 1.94 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653096B2
Source datasetuspto-grants-2014_02
ORD IDord-43edd3001e344c21a7c8c83a3da5523e
Source noteuspto-grants-2014_02