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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432583Generated: October 31, 2026

Ammonia → 4-{[(tert-Butoxycarbonyl)amino]methyl}-3-chlorobenzoic acid

https://huagongshe.com/reaction/432583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantSodium HydroxideHCID 14798—
ReactantDi-tert-butyl dicarbonateHCID 90495—
ReactantMethyl 4-(bromomethyl)-3-chlorobenzoateHCID 22027761—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product4-{[(tert-Butoxycarbonyl)amino]methyl}-3-chlorobenzoic acidHCID 22027774—

Reaction Steps

To a saturated solution of ammonia in ethanol (170 ml) was added methyl 4-bromomethyl-3-chlorobenzoate from Example A1 (5.5 g, 20.9 mmol). The mixture was stirred at room temperature for 1 h and then concentrated in vacuo. The residue was triturated with diethyl ether and the resultant white crystals were filtered off and washed with more diethyl ether. To a solution of this solid in water (100 ml) were added solutions of (BOC)2O (5.0 g, 23.0 mmol) in dioxan (100 ml) and sodium hydroxide (1.86 g, 46.0 mmol) in water (100 ml). The mixture was stirred at room temperature for 18 h and then concentrated in vacuo. The aqueous residue was acidified with citric acid and extracted with chloroform/IPA. The organic layer was washed with water, dried over MgSO4, and concentrated in vacuo to give a white solid; yield 2.8 g (67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06664249B1
Source datasetuspto-grants-2003_12
ORD IDord-7dc800cb4e704341a76d42a433e113e1
Source noteuspto-grants-2003_12