HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 974603Generated: October 25, 2026
Methylamine → 3-(4-Fluorophenoxy)-N-methyl-1-azetidinecarboxamide
https://huagongshe.com/reaction/974603
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 3-(4-Fluorophenoxy)-1-azetidinecarbonyl chloride | HCID 15053367 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(4-Fluorophenoxy)-N-methyl-1-azetidinecarboxamide | HCID 15053437 | 129.3% |
Reaction Steps
A solution of 4.6 g (0.02 mole) of 3-(4-fluorophenoxy)-1-azetidinecarbonyl chloride in 15 ml of tetrahydrofuran was stirred while 6.2 g (0.08 mole) of 40% aqueous methylamine was added. The reaction mixture was exothermic and was allowed to cool to ambient temperature while stirring for 18 hr. The reaction mixture was diluted with 200 ml of ice water and the oil droplets which separated quickly crystallized. Filtration yielded 6.6 g of crude product. The solid was dissolved in 100 ml of methylene chloride, treated with 15 g of silica gel and stirred for 2 hr. The silica gel was removed by filtration and washed wit 200 ml of 50/50 ethyl acetatemethylene chloride. The combined filtrates were concentrated on a rotary evaporator, yielding 5.8 g of solid residue. The solid was recrystallized by dissolving in 22 ml of acetone and adding 88 ml of isopropyl ether. The volume was reduced to 40 ml by boiling under nitrogen atmosphere and upon cooling the product crystallized. Filtration yielded 2.95 (66.7%) of white crystals, m.p. 140°-142° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05068231 |
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| Source dataset | uspto-grants-1991_11 |
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| ORD ID | ord-f75f0d7ea04c43aaa84e1e4db2741c27 |
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| Source note | uspto-grants-1991_11 |
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