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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1983781Generated: November 3, 2026

Acetic Acid → HCID 66758387, compound

https://huagongshe.com/reaction/1983781

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) 6: 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 numberUS07541365B2
Source datasetuspto-grants-2009_06
ORD IDord-2c695e85c5d04b2bb6c3566e464e3da0
Source noteuspto-grants-2009_06