HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylamine → 3-(2-Chloro-6-methylphenoxy)-N,N-dimethyl-1-azetidinecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | 3-(2-Chloro-6-methylphenoxy)-1-azetidinecarbonyl chloride | HCID 15042231 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(2-Chloro-6-methylphenoxy)-N,N-dimethyl-1-azetidinecarboxamide | HCID 19906220 | — |
Reaction Steps
A stirred solution of 3.9 g (0.015 mole) of 3-(2-chloro-6-methylphenoxy)-1-azetidinecarbonyl chloride in 20 mL of tetrahydrofuran was treated all at once with 5.1 mL (0.045 mole) of 40% aqueous dimethylamine. After stirring for 72 h the raction mixture was diluted with 200 mL of water and the oil which separated was extracted into methylene chloride (3×30 mL). The combined extracts were dried by filtering through Whatman PS paper and concentrated in vacuo (3.6 g). The crude oil solidified when cooled in a dry ice/acetone bath and was recrystallized from ethyl ether in a dry ice-acetone bath yielding, after filtering cold, 2.6 g (64.5%) of coarse white crystals, mp 46°-47° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05095014 |
| Source dataset | uspto-grants-1992_03 |
| ORD ID | ord-93fc2324eaff467195c451fec22d493d |
| Source note | uspto-grants-1992_03 |