HuagongsheHuagongshe Chemistry Print Report · For research reference only
Adamantane → Adamantane-1-sulfinyl Chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Adamantane | HCID 9238 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | Adamantane-1-sulfinyl Chloride | HCID 4737333 | — |
Reaction Steps
Aluminum trichloride (40 g, 3 mol) was added slowly to thionyl chloride (200 ml, 2.7 mol), and the mixture was cooled to -20°. Adamantane was added in portions over 21/2 hrs, and the resulting mixture was stirred 1 hr and allowed to warm to room temperature. After the thionyl chloride was removed under vacuum, the residue was diluted with CCl4 ; and the aluminum trichloride was decomposed with ice and water. The layers were separated; and the organic layer was washed (brine), dried (Na2SO4), filtered, and concentrated under vacuum. The residue was distilled under vacuum (1 torr, 133.3 Pascals) with a vigreaux column to give the product (28.8 g; bp 118°-128°) as a waxy solid; TLC, Rf =0.6-0.4, EtOAc:hexanes (15:85).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05414132 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-132d52926e864bb082d78664c42f3ae1 |
| Source note | uspto-grants-1995_05 |