HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxylamine → 2-Thiabicyclo[3.2.2]non-5-en-3-one oxime
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxylamine | HCID 787 | — |
| Reactant | Cyclohexane | HCID 8078 | — |
| Reactant | Thiophosgene | HCID 10040 | — |
| Reactant | 1,3-Cycloheptadiene | HCID 19969 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Thiabicyclo[3.2.2]non-5-en-3-one oxime | HCID 86739166 | — |
Reaction Steps
A solution of 29 g (0.3 m) of 1,3-cycloheptadiene, 46 g (0.4 m) of thiophosgene, and 25 ml of cyclohexane was heated under reflux for 24 hours, then stripped of volatiles under reduced pressure. The oily residue was taken up in 150 ml of methylene chloride and stirred with 1.5 m of hydroxylamine in 200 ml of water at room temperature for three days. The separated organic layer was dried over magnesium sulfate and stripped to yield 26.7 g of viscous oil. Purification by dry column chromatography using silica gel and 1:4::ether:hexane as eluent. There was obtained 14 g of yellow solid. Recrystallization of 2 g portion from 1:1 ether-hexane yielded 1.4 g of the title compound as white crystals, m. 130°-132° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04548929 |
| Source dataset | uspto-grants-1985_10 |
| ORD ID | ord-754600ee85d34f2098b845d6aab14c79 |
| Source note | uspto-grants-1985_10 |