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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441540Generated: November 1, 2026

Oxygen → 2-Acetylamino-5-formyl-4-trifluoromethyl-benzoic acid methyl ester

https://huagongshe.com/reaction/1441540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxygenHCID 977—
ReactantDimethyl SulfideHCID 1068—
ReactantTriphenylphosphineHCID 11776—
ReactantOzoneHCID 24823—
ReactantHCID 59164494HCID 59164494—
SolventDichloromethaneHCID 6344—
Product2-Acetylamino-5-formyl-4-trifluoromethyl-benzoic acid methyl esterHCID 5916442383%

Reaction Steps

A solution of 2-acetylamino-4-trifluoromethyl-5-vinyl-benzoic acid methyl ester (708 mg, 2.46 mmol) in DCM (70 mL) was cooled to −68° C. and a flow of ozone was passed through the mixture until it turned dark green. A flow of oxygen was then passed through the mixture for 30 min and dimethyl sulfide (360 μL, 4.86 mmol) was added. This mixture was stirred for 30 min at r.t. and triphenylphosphine (327 mg, 1.23 mmol) was added. The solution was allowed to stand for 60 h at r.t. under argon. It was then concentrated in vacuo and the crude product was purified by flash chromatography (silica gel 60, hexanes/EtOAc 100:0→80:20) to afford 2-acetylamino-5-formyl-4-trifluoromethyl-benzoic acid methyl ester (591 mg, 2.04 mmol, 83%) as a beige powder, m.p. 106-108° C., ESI-MS: m/z 290 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07655666B2
Source datasetuspto-grants-2010_02
ORD IDord-c6db558cebdf43c9b060a71c3df5cf2b
Source noteuspto-grants-2010_02