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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010057Generated: November 1, 2026

Trimethylsilyldiazomethane → 4-Amino-3-chloro-2-fluoro-5-nitro-benzoic acid methyl ester

https://huagongshe.com/reaction/1010057

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyldiazomethaneHCID 167693—
Reactant4-Amino-3-chloro-2-fluoro-5-nitro-benzoic acidHCID 21114182—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product4-Amino-3-chloro-2-fluoro-5-nitro-benzoic acid methyl esterHCID 8586819439.4%

Reaction Steps

To a stirred solution of 4-amino-3-chloro-2-fluoro-5-nitro-benzoic acid 3a (3.61 g, 15.4 mmol) in THF (30 mL) and MeOH (10 mL), TMS diazomethane (9.23 mL, 2.0 M solution in hexanes, 18.5 mmol) is added. After completion of reaction, the reaction mixture is concentrated via rotary evaporation with acetic acid in the trap. The recovered oily solid is triturated with diethyl ether to provide 1.51 g of a yellow solid. The filtrate is concentrated and triturated with diethyl ether to give an additional 0.69 g of yellow solid. A total of 2.20 g (57%) of pure desired product is recovered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973170B2
Source datasetuspto-grants-2011_07
ORD IDord-bce5bb0f15654e848f21ffecd3764f6d
Source noteuspto-grants-2011_07