HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371727Generated: October 31, 2026
Phosgene → 3-[2-Fluoro-5-(trifluoromethyl)phenoxy]-1-azetidinecarbonyl chloride
https://huagongshe.com/reaction/2371727
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(Diphenylmethyl)-3-[2-fluoro-5-(trifluoromethyl)phenoxy]azetidine | HCID 19906227 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-[2-Fluoro-5-(trifluoromethyl)phenoxy]-1-azetidinecarbonyl chloride | HCID 15042233 | 163.3% |
Reaction Steps
A mixture of 10.8 g (0.11 mole) of phosgene and 14.2 g (0.11 mole) of potassium carbonate in 200 mL of methylene chloride was cooled to 5° C. in an ice bath while stirring undr nitrogen. After 30 min, the reaction mixture was treated with 40 g (0.1 mole) of 1-(diphenylmethyl)-3-[2-fluoro-5-(trifluoromethyl)phenoxy]azetidine in 100 mL of methylene chloride added dropwise. After stirring for 16 h, the reaction mixture was treated with small pieces of ice to destroy any excess phosgene. Then the reaction mixture was decanted from the inorganic paste and concentrated in vacuo to give 48.6 g of pale yellow oil. The residual oil was distilled at 0.15 mmHg to yield 3 fractions: #1, 12.7 g at 120°-128°; #2, 1.5 g at 128°, and #3 at 128°-132°; with total yield of 19.7 g (66.2%). A sample of fraction #2 was submitted for analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05095014 |
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| Source dataset | uspto-grants-1992_03 |
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| ORD ID | ord-1f2211643d4d4312b70bea3b5be5d3b9 |
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| Source note | uspto-grants-1992_03 |
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