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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1435153Generated: October 31, 2026

Acetic Acid → 3-[(2,4-Dichlorobenzylamino)-methyl]-azetidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1435153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant2,4-DichlorobenzaldehydeHCID 13404—
ReactantSodium HydroxideHCID 14798—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantTert-butyl 3-(aminomethyl)azetidine-1-carboxylateHCID 10679125—
Solvent1,2-DichloroethaneHCID 11—
Product3-[(2,4-Dichlorobenzylamino)-methyl]-azetidine-1-carboxylic acid tert-butyl esterHCID 6900297765.2%

Reaction Steps

To a solution of 3-aminomethyl-azetidine-1-carboxylic acid tert-butyl ester (300 mg, 1.6 mmol), 2,4-dichlorobenzaldehyde (281 mg, 1.61 mmol) and acetic acid (0.09 mL, 1.61 mmol) in 1,2-dichloroethane (16 mL) at 0° C. is added sodium triacetoxy-borohydride (476 mg, 2.25 mmol). The reaction is warmed to ambient temperature and stirred overnight under N2. The reaction mixture is poured on to 2N NaOH (20 mL) and extracted with ethyl acetate (3×). The combined organic extracts are washed with aqueous saturated NaCl, dried (Na2SO4), filtered and concentrated. The crude product is purified by flash chromatography on silica gel eluting with 5% EtOH (10% NH4OH)/chloroform to yield 360 mg (65%) of 3-[(2,4-dichlorobenzylamino)-methyl]-azetidine-1-carboxylic acid tert-butyl ester. 1H NMR (400 MHz, CD3OD) δH: 7.49-7.47 (2H, m), 7.36-7.34 (1H, m), 4.05-4.01 (2H, m), 3.88 (2H, s), 3.64-3.61 (2H, m), 2.8 (2H, m), 2.78-2.74 (1H, m), 1.46 (9H, s). Mass spectrum (ion spray): m/z=345.1 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07615648B2
Source datasetuspto-grants-2009_11
ORD IDord-909bc2b191724333b1458f9363f4df5b
Source noteuspto-grants-2009_11