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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482013Generated: October 29, 2026

Trimethylsilyldiazomethane → methyl 2-amino-4-chloro-5-methoxybenzoate

https://huagongshe.com/reaction/482013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyldiazomethaneHCID 167693—
Reactant2-AMino-4-chloro-5-Methoxy-benzoic acidHCID 19064965—
SolventMethanolHCID 887—
Productmethyl 2-amino-4-chloro-5-methoxybenzoateHCID 1906493346%

Reaction Steps

A solution of 2-amino-4chloro-5-methoxybenzoic acid (3.0 g, 15.0 mmol; prepared according to the procedure of Denny, et al., J. Med. Chem. 34:217-222 (1991)) in 70 ml MeOH was treated with excess trimethylsilyl diazomethane. The solution was concentrated and the residue flash chromatographed on silica (9:1 hexane/EtOAc to give the title compound (46%): mp 63°-64° C.; 1H NMR (300 MHz, CDCl3) δ 6 3.83 (s, 3H), 3.90 (s, 3H), 5.48 (bs, 2H), 6.75 (s, 1H), 7.39 (s, 1H); MS (DCI/NH3) m/z 216 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05792767
Source datasetuspto-grants-1998_08
ORD IDord-2051251030fc40e2983054b5acb85699
Source noteuspto-grants-1998_08