HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-Bromo-2-chlorobenzyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | (4-Bromo-2-chlorophenyl)methanol | HCID 43805739 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Bromo-2-chlorobenzyl methanesulfonate | HCID 22058649 | — |
Reaction Steps
To a solution of 4-bromo-2-chlorobenzyl alcohol (3.56 g) and anhydrous triethylamine (3 ml) in anhydrous dichloromethane (36 ml) was dropwise added methanesulfonyl chloride (1.4 ml) under a nitrogen atmosphere and ice-cooling. The reaction mixture was stirred for 1 hr, washed with water, a saturated aqueous sodium hydrogencarbonate solution and saturated brine, and dried over anhydrous magnesium sulfate. The filtrate was concentrated to give the objective compound (4.77 g) as a light brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06911469B2 |
| Source dataset | uspto-grants-2005_06 |
| ORD ID | ord-e9ea002048984dc8a307a503c020fd6d |
| Source note | uspto-grants-2005_06 |