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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095861Generated: November 3, 2026

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

https://huagongshe.com/reaction/1095861

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 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) δ 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 numberUS08138189B2
Source datasetuspto-grants-2012_03
ORD IDord-9b8dc8a50fb54aba9834a80cec6cd526
Source noteuspto-grants-2012_03