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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2353168Generated: November 4, 2026

Acetyl chloride → Methyl 3-Amino-4-chlorobenzoate

https://huagongshe.com/reaction/2353168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyl chlorideHCID 6367—
Reactant3-Amino-4-chlorobenzoic acidHCID 76092—
SolventMethanolHCID 887—
ProductMethyl 3-Amino-4-chlorobenzoateHCID 593055—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 4-chloro-3-amino-benzoic acid (10.0 g, 58.3 mmol) in methanol (50 mL) was added acetyl chloride (13.0 mL) dropwise at room temperature. After the addition, the reaction mixture was heated at 70° C. for 3 h and then cooled to room temperature. The solvent was removed under reduced pressure and water (100 mL) was added. The resulting solution was neutralized with NaHCO3 followed by extraction with EtOAc (3×100 mL). The combined organic layers were dried (MgSO4) and concentrated in vacuum to afford a yellow oil (22, 10.5 g, 97%). 1H NMR (DMSO-d6, 300 MHz) δ 7.41 (??d, J=2.1 Hz, 1H), 7.31 (d, J=8.4 Hz, 1H), 7.09 (dd, J=2.1, 8.4 Hz, 1H), 5.66 (br s, 2H), 3.80 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750008B2
Source datasetuspto-grants-2010_07
ORD IDord-e643973059764eaa9e053322739d9a32
Source noteuspto-grants-2010_07