Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992278Generated: October 31, 2026

Trifluoroacetic acid → HCID 57948959, compound

https://huagongshe.com/reaction/1992278

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 68539143HCID 68539143—
SolventMethanolHCID 887—
ProductHCID 57948959HCID 5794895962%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of (S)-tert-butyl 4-(3-bromo-4-fluorophenyl)-4-methyl-5,6-dihydro-4H-1,3-thiazin-2-ylcarbamate (1.1 g, 2.7 mmoles) and methanol (10 mL) is added trifluoroacetic acid (10 mL). The reaction mixture is warmed to 60° C. After 15 h, the solvent is removed under reduced pressure. Water is added to the resulting residue and the mixture is made basic with saturated sodium bicarbonate. The basic aqueous phase is extracted with dichloromethane. The organic phase is separated, dried over sodium sulfate, filtered, and the solvent removed under reduced pressure to give the title compound (62% yield): MS (m/z): 303, 305 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07648983B2
Source datasetuspto-grants-2010_01
ORD IDord-6b5b9a9dd65b485ebbfd38b5005f22c8
Source noteuspto-grants-2010_01