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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113368Generated: November 2, 2026

4-Amino-5-chloro-2-methoxybenzoic acid → Methyl 4-amino-5-chloro-2-methoxybenzoate

https://huagongshe.com/reaction/2113368

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-5-chloro-2-methoxybenzoic acidHCID 81626—
ReactantTrimethylsilyldiazomethaneHCID 167693—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
ProductMethyl 4-amino-5-chloro-2-methoxybenzoateHCID 700493—

Reaction Steps

To a solution of 4-amino-5-chloro-2-methoxybenzoic acid (1.008 g, 5.0 mmol) in a mixture of toluene (9 mL) and methanol (1 mL) at 0° C. was added (trimethylsilyl)diazomethane (2.0 M in hexane, 3.0 mL, 6.0 mmol) dropwise. The reaction mixture was then warmed to room temperature and stirred for 16 h. Excess (trimethylsilyl)diazomethane was quenched by adding acetic acid until the bright yellow color of the reaction mixture disappeared. The mixture was then concentrated in vacuo to give the title compound as an off-white solid, which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524959B2
Source datasetuspto-grants-2009_04
ORD IDord-80c4199b2e5d402cbc5895da10d255b2
Source noteuspto-grants-2009_04