HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propionyl chloride → 4-(3-Bromopropylthio)phenylpropan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propionyl chloride | HCID 62324 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 3-Bromopropyl phenyl sulfide | HCID 7061847 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(3-Bromopropylthio)phenylpropan-1-one | HCID 14650281 | — |
Reaction Steps
To a solution of thioether from Example 1, (460 g, 2 moles) and propionyl chloride (202 g, 2.2 moles) in dichloromethane (8 L) at -15° C. was added in portions of approximately 30 g over 1 hour, aluminum chloride (320 g, 2.4 moles). After two hours at -15° C. the reaction mixture was quenched with ice until it became colorless. 1N HCl (2 L) was added and the reaction mixture was stirred until two clear phases were obtained (approximately 30 minutes). The organic layer was siphoned off and dried (Na2SO4). Evaporation afforded an oil which crystallized upon addition of hexane (2 L) and cooling in ice water bath; yield 470 g, m.p. 40°-41° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04857659 |
| Source dataset | uspto-grants-1989_08 |
| ORD ID | ord-9c0f3f7046344989b041d75962298cf3 |
| Source note | uspto-grants-1989_08 |