HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216404Generated: October 29, 2026
Acetic Anhydride → HCID 178506310, compound
https://huagongshe.com/reaction/216404
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178520388 | HCID 178520388 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178506310 | HCID 178506310 | — |
Reaction Steps
A suspension of (2R)-1,1,1-trifluoro-2-[4-(1H-pyrazol-1-yl)phenyl]-3-(4-{[1-(trifluoromethyl)cyclopropyl]methyl}-1H-imidazol-2-yl)propan-2-ol in acetic acid (10 mL)/acetic anhydride (10 mL) was heated to reflux. The reaction mixture was poured into 1M sodium hydroxide solution until basic and extracted with diethyl ether. The crude product was dissolved in a mixture of methanol and acetonitrile and charged with 1M sodium hydroxide. It was heated to reflux overnight, and the reaction mixture was extracted with diethyl ether. The combined organic extracts were washed with brine, dried (potassium carbonate) and concentrated in vacuo to afford 1-{4-[(Z)-1-(trifluoromethyl)-2-(4-{[1-(trifluoromethyl)cyclopropyl]methyl}-1H-imidazol-2-yl)vinyl]phenyl}-1H-pyrazole, which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193228B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-025df225d1694e3580d3d9118408d1a6 |
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| Source note | uspto-grants-2012_06 |
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