HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974545Generated: October 26, 2026
Water → 3-(4-Fluorophenoxy)-1-azetidinecarbonyl chloride
https://huagongshe.com/reaction/974545
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Benzhydryl-3-(4-fluorophenoxy)azetidine | HCID 15053369 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(4-Fluorophenoxy)-1-azetidinecarbonyl chloride | HCID 15053367 | — |
Reaction Steps
A solution of 52.09 g (0.527 mole) of phosgene in 500 ml of methylene chloride was stirred with 73 g (0.53 mole) of potassium carbonate under nitrogen atmosphere for 30 min, then treated with 146.3 g (0.439 mole) of 1-diphenylmethyl-3-(4-fluorophenoxy)azetidine in 300 ml of methylene chloride added dropwise. After stirring for 18 hr, the reaction mixture was treated with 200 ml of water added slowly. The aqueous phase was separated and the organic solution dried by filtration through Whatman phase separating filter paper then concentrated in vacuo to a pale amber oil. Trituration of the oil with 30/60 petroleum ether yielded a crude tacky solid, 89.3 g (88.6%). A portion of this solid was recrystallized from 30/60 petroleum ether yielding a fine white crystalline product, m.p. 44°-52° C. A second recrystallization from isopropyl ether yielded fine white crystals, m.p. 57°-58.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05068231 |
|---|
| Source dataset | uspto-grants-1991_11 |
|---|
| ORD ID | ord-c79644b79d5a48aea1c5f779fe3709ef |
|---|
| Source note | uspto-grants-1991_11 |
|---|