HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Bis(4-bromobenzyl)sulfide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Bromobenzyl bromide | HCID 68527 | — |
| Reactant | (4-Bromophenyl)methanethiol | HCID 271218 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Bis(4-bromobenzyl)sulfide | HCID 12328857 | 91% |
Reaction Steps
To a solution of 1.85 g (9.11 mmol) of 4-bromobenzylmercaptan in dry dichloromethane (30 ml) were added 2.72 g (10.9 mmol) of 4-bromobenzyl bromide and 2.31 g (22.8 mmol) of triethylamine in an atmosphere of argon, and the mixture was allowed to react at room temperature for 16 hours. To the solution was added water followed by extraction with ethyl acetate. The organic layer was washed with water and then concentrated under reduced pressure. The residue thus obtained was subjected to silica gel column chromatography for separation and purification. Elution with ethyl acetate-hexane (1:4) yielded 3.08 g (8.29 mmol) of bis(4-bromobenzyl)sulfide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05043142 |
| Source dataset | uspto-grants-1991_08 |
| ORD ID | ord-5b2e5695cf634031a6e633db2c3b5008 |
| Source note | uspto-grants-1991_08 |