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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386476Generated: October 30, 2026

Acetic Acid → (3-Benzylamino-phenyl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/386476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantBenzaldehydeHCID 240—
ReactantSodium borohydrideHCID 4311764—
Reactanttert-butyl N-(3-aminophenyl)carbamateHCID 12877220—
SolventTetrahydrofuranHCID 8028—
Product(3-Benzylamino-phenyl)-carbamic acid tert-butyl esterHCID 67229700—

Reaction Steps

A solution of (3-amino-phenyl)-carbamic acid tert-butyl ester (1 g, 4.8 mmol), benzaldehyde (0.54 ml, 5.3 mmol) and acetic acid (0.41 ml, 7.2 mmol) in dry tetrahydrofuran (30 ml) were stirred at room temperature for 2 hrs. Sodium borohydride (0.172 g, 4.5 mmol) was added and the reaction stirred at room temperature overnight. The reaction mixture was quenched with water (50 ml) and extracted with dichloromethane (3×50 ml). The combined organics were dried (magnesium sulphate), concentrated in vacuo and the crude residue purified by flash column chromatography (SiO2) eluting with ethyl acetate to afford the title compound as an off white solid (1.27 g, 89%) HPLC retention time 6.4 min. Mass spectrum (ES+) m/z 198 (M+H-BOC)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372840B2
Source datasetuspto-grants-2013_02
ORD IDord-6d428428c64741a0a9545bbc31f9dadf
Source noteuspto-grants-2013_02