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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1629747Generated: November 3, 2026

Sodium triacetoxyborohydride → 1-(5-Bromo-2-chloro-benzyl)azetidine-3-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1629747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant5-Bromo-2-chlorobenzaldehydeHCID 10608925—
Reactanttert-Butyl azetidine-3-carboxylate hydrochlorideHCID 67346984—
SolventDichloromethaneHCID 6344—
Solvent1,1-DichloroethaneHCID 6365—
Product1-(5-Bromo-2-chloro-benzyl)azetidine-3-carboxylic acid tert-butyl esterHCID 58374422—

Reaction Steps

A mixture of 5-bromo-2-chloro-benzaldehyde (2 g, 9.11 mmol) and azetidine-3-carboxylic acid tert-butyl ester hydrochloride (1.765 g, 9.11 mmol) in dichloroethane (50 mL) was stirred at room temperature for 10 minutes. To this mixture was added sodium triacetoxy-borohydride (3.86 g, 18.23 mmol) in 3 portions over a period of 10 minutes and the cloudy mixture was stirred overnight. The reaction mixture was diluted with CH2Cl2 (100 mL) and washed twice with 10% sodium bicarbonate solution, twice with water then brine. The organic layer was dried over sodium sulfate, filtered and concentrated. The crude was purified by chromatography on silica gel (cyclohexane/EtOAc).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791100B2
Source datasetuspto-grants-2014_07
ORD IDord-61c9ca146a9b43c2a3e4ff852a0bb7a1
Source noteuspto-grants-2014_07