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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347625Generated: October 31, 2026

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

https://huagongshe.com/reaction/347625

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 hr and then concentrated in vacuo. The residue was triturated with diethyl ether and the resultant white crystals were fiflered 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 numberUS07176195B2
Source datasetuspto-grants-2007_02
ORD IDord-16931e280b954d89a12c8c93d7696010
Source noteuspto-grants-2007_02