HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164529Generated: October 26, 2026
Acetyl chloride → N-Formyl-3-[3-(trifluoromethyl)phenoxy]azetidine-1-carboxamide
https://huagongshe.com/reaction/2164529
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Acetic-formic anhydride | HCID 75269 | — |
| Reactant | Dezinamide | HCID 146291 | — |
| Reactant | Sodium Formate | HCID 2723810 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-Formyl-3-[3-(trifluoromethyl)phenoxy]azetidine-1-carboxamide | HCID 13476971 | 61% |
Reaction Steps
A mixture of 0.524 g (0.002 mole) of 3-[3-(trifluoromethyl)phenoxy]-1-azetidinecarboxamide and 1.5 ml of formic acetic anhydride (prepared by reacting sodium formate and acetyl chloride in ether at 23°-27° C. for 5.5 hr, filtering and evaporating off the ether) was stirred at room temperature for about 54 hr. The mixture was evaporated to dryness and the residue was partitioned between 7 ml methylene chloride and 2 ml water. The methylene chloride layer was separated, dried over sodium sulfate and evaporated to dryness. The residue was triturated with ether and the mixture subjected to filtration to give a solid white filter cake weighing 0.398 g after drying. The solid was stirred with more ether for 10 minutes and the mixture filtered to give 0.350 g (61%) white powder, m.p. 117.5°-119° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04505907 |
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| Source dataset | uspto-grants-1985_03 |
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| ORD ID | ord-5555b1059e1a4b9a9cf1b9d706cc933c |
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| Source note | uspto-grants-1985_03 |
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