HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromobenzenethiol → 1-Bromo-2-[(2-chloropentyl)sulfanyl]benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromobenzenethiol | HCID 80598 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 13663922 | HCID 13663922 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Bromo-2-[(2-chloropentyl)sulfanyl]benzene | HCID 21393397 | 95.2% |
Reaction Steps
To a solution of 23.0 g of sodium metal is 500 ml of absolute ethanol is added, in about 0.5 hour, a solution of 173.0 g of o-bromothiophenol in 250 ml of absolute ethanol. The mixture is stirred and heated under reflux for about 0.5 hour, cooled to 0°, and treated, dropwise, with 185.5 g of 1-bromo-2-chloropentane. The addition requires about 1 hour. The mixture is stirred for about 2 hours at 0°, warmed slowly to reflux, and then heated under reflux for 2 hours. The mixture is filtered and the filtrate concentrated in vacuo at 40° to give about 255.7 g of o-bromophenyl 2-chloro-1-pentyl sulfide as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03966733 |
| Source dataset | uspto-grants-1976_06 |
| ORD ID | ord-5e990209d35b480094f83b31cccef0aa |
| Source note | uspto-grants-1976_06 |