HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → HCID 13923222, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 178450332 | HCID 178450332 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | HCID 13923222 | HCID 13923222 | 84% |
Reaction Steps
420 ml of oxalyl chloride were added at 0° to 5° C. to 141.2 g (0.5 mol) of 2-butyryl-3-hydroxy-5-(tetrahydrothiopyran-3-yl)cyclohex-2-en-1-one, and the mixture was stirred at room temperature for 16 hours and concentrated. The oil obtained was treated with methyl tert.-butyl ether, and the resulting solid was filtered off with suction and dried. This gave 125.9 g (84% yield) of 2-butyryl-3-chloro-5-(tetrahydrothiopyran-3-yl)cyclohex-2-en-1-one having a melting point of 97° C. (decomposition) (compound no. 312).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04761486 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-a014d6e381fe4f1ba33060fdff7657ff |
| Source note | uspto-grants-1988_08 |