HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl Mercaptan → 4-Allylthioazetidin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl Mercaptan | HCID 13367 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Acetoxy-2-azetidinone | HCID 119981 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Allylthioazetidin-2-one | HCID 12849630 | — |
Reaction Steps
A solution of 42.9 g of sodium hydroxide in 500 ml of water was made up under nitrogen and cooled to room temperature, 108 ml of allyl mercaptan was added and the mixture stirred under nitrogen for 30 minutes. 138.7 g of 4-acetoxyazetidin-2-one was added to the mixture over 10 minutes under nitrogen and the reaction mixture was stirred overnight in an air atmosphere. The reaction mixture was extracted into dichloromethane (6×250 ml). The organic layer was washed with water (2×250 ml), dried over magnesium sulphate and evaporated in vacuo to dryness. Purification, over silica gel and elution with hexane-ethylacetate, afforded the above product as a yellow oil. (112.1 g, 73% of the theoretical yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04684640 |
| Source dataset | uspto-grants-1987_08 |
| ORD ID | ord-dad2eed20186402398cc850a972487d1 |
| Source note | uspto-grants-1987_08 |