HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992278Generated: October 31, 2026
Trifluoroacetic acid → HCID 57948959, compound
https://huagongshe.com/reaction/1992278
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 68539143 | HCID 68539143 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 57948959 | HCID 57948959 | 62% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07648983B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-6b5b9a9dd65b485ebbfd38b5005f22c8 |
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| Source note | uspto-grants-2010_01 |
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