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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2229756Generated: November 1, 2026

3-Chlorophenylacetic acid → HCID 14918164, compound

https://huagongshe.com/reaction/2229756

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chlorophenylacetic acidHCID 15879—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
ReactantDiisopropylethylamineHCID 81531—
SolventDichloromethaneHCID 6344—
ProductHCID 14918164HCID 14918164—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 3-chlorophenylacetic acid (5.00 g, 29.3 mmol), 1-(3-dimethyl-aminopropyl)-3-ethylcarbodiimide HCl (6.18 9, 32.2 mmol), and 1-hydroxybenzotriazole (HOBt; 4.00 9, 29.3 mmol) in dichloromethane (DCM; 40 mL) was stirred at room temperature for about 10 minutes. The solution was cooled to about 0° C. To it were added N,O-dimethylhydroxylamine HCl (2.86 g, 29.0 mmol) and diisopropylethylamine (DIEA; 3.80 g, 29.3 mmol). The reaction mixture was warmed to room temperature and stirred for about 5 hours. The solution was diluted with 100 mL of DCM and washed with saturated NaHCO3 aqueous solution (2 times), iN HCl aqueous solution (2 times) and brine (2 times), dried over anhydrous MgSO4, filtered and concentrated in vacuo. The liquid obtained was purified by column chromatography on silica eluting with EtOAc/hexane 1:1. The title compound was obtained as colorless liquid. Yield: 5.60 g, 89%. Rf=0.44 (silica, EtOAc/hexane 1:1). 1H NMR (300 MHz, CDCl3) 7.18-7.34 (m, 4H), 3.76 (S, 2H), 3.66 (S, 3H), 3.22 (S, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06420555B1
Source datasetuspto-grants-2002_07
ORD IDord-201e1cd9278e4803a3f0881e2f028504
Source noteuspto-grants-2002_07