HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Benzene, 1-butyl-4-(chloromethyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 4-Butylbenzyl alcohol | HCID 578288 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzene, 1-butyl-4-(chloromethyl)- | HCID 182273 | 82% |
Reaction Steps
Methanesulfonyl chloride (3.069 g, 26.791 mmol) was added to a solution of 4-butylbenzyl alcohol (4.000 g, 24.355 mmol) in dichloromethane (120 mL) at 0° under argon atmosphere. Triethylamine (2.711 g, 26.791 mmol) was added dropwise at a slow speed to this mixture, and stirred at room temperature overnight. The solvent was evaporated under reduced pressure and the residue was diluted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. The residue obtained by evaporation of the solvent under reduced pressure was purified by column chromatography on silica gel (n-hexane) to give the title compound (3.64 g, 82%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07884234B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-44fc922bf5fb4da5aa95292bbdaba2c0 |
| Source note | uspto-grants-2011_02 |