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 added dropwise methanesulfonyl chloride (1.4 ml) under ice-cooling in a nitrogen atmosphere. The mixture was stirred for 1 hr, and the reaction mixture was washed with water, saturated aqueous sodium hydrogencarbonate solution and saturated brine, and dried over anhydrous magnesium sulfate. The filtrate was concentrated to give 4-bromo-2-chloro-1-((methanesulfonyloxy)-methyl)benzene as a pale-brown solid (4.77 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07060721B1 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-4aa4643bf50f4c25be47a1f1df94a7f0 |
| Source note | uspto-grants-2006_06 |