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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488946Generated: October 29, 2026

Ethyl chloroformate → HCID 22268766, compound

https://huagongshe.com/reaction/488946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 22268778HCID 22268778—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22268766HCID 22268766—

Reaction Steps

Methyl 3-amino-5-(trifluoromethyl)benzoate (cf. procedures (116a) and (80a); 236 mg, 1.01 mmol) was dissolved in THF (11 mL) and the resulting solution was charged successively with K2CO3 (1.6 mL of a 2.0 M aq. solution) and ethylchloroformate (258 mg, 2.7 mmol). The reaction was stirred at RT for 48 h, concentrated in vacuo, and diluted with EtOAc. The organic phase was washed with sat. NaHCO3, water (2×), and brine before being dried (Na2SO4), filtered, and concentrated in vacuo. This product was dissolved in 3:1 THF/MeOH (8 mL) and the resultant solution was charged with lithium hydroxide (2 mL of a 1N solution). The reaction was stirred for 14 h, acidified with 1N HCl, and extracted with EtOAc (2×). The organic extracts were combined, washed with water, washed with brine, dried (Na2SO4), filtered, and concentrated in vacuo to provide 3-(ethoxycarbonyl)amino-5-(trifluoromethyl)benzoic acid. MS found: (M−H)−=276.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06974836B2
Source datasetuspto-grants-2005_12
ORD IDord-3ef7f034819f42249018a6d26848780c
Source noteuspto-grants-2005_12