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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333756Generated: October 29, 2026

1,2-Dichloroethane → 2-Chloro-4-methoxyphenylacetic acid ethylester

https://huagongshe.com/reaction/333756

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantEthanolHCID 702—
ReactantTriethylamineHCID 8471—
Reactant2-(2-Chloro-4-methoxyphenyl)acetic acidHCID 4209132—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product2-Chloro-4-methoxyphenylacetic acid ethylesterHCID 5738350864%

Reaction Steps

Ethanol (8.72 mL, 150 mmol), DMAP (304 mg, 2 mmol), EDC (9.56 g, 50 mmol), and triethylamine (6.91 mL, 50 mmol) were added under cooling (ice) to a solution of (2-chloro-4-methoxy-phenyl)-acetic acid (10.00 g, 50 mmol, [CAS Reg. No. 91367-09-8]) in CH2Cl2 (200 mL). The reaction mixture was stirred at r.t. overnight, then diluted (CH2Cl2), and washed (1N aqueous HCl). The organic layer was dried (Na2SO4), and the solvent was evaporated. Purification of the residue by column chromatography (silica gel, heptane:ethyl acetate=100:0-70:30) gave the title compound (7.27 g, 64%). 1H NMR (300 MHz, CDCl3) 7.18 (1H, d), 6.94 (1H, d), 6.79 (1H, dd), 4.17 (2H, q), 3.79 (3H, s), 3.69 (2H, s), 1.26 (3H, t).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883786B2
Source datasetuspto-grants-2014_11
ORD IDord-e40d289f8e6d4d229db6b30621283e76
Source noteuspto-grants-2014_11