HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-(4-Chlorophenyl)-3-(3-cyanophenyl)-2-methylsulfonyloxybutane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 4-(4-Chlorophenyl)-3-(3-cyanophenyl)-2-butanol | HCID 11529339 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-(4-Chlorophenyl)-3-(3-cyanophenyl)-2-methylsulfonyloxybutane | HCID 57438715 | — |
Reaction Steps
To a solution of 4-(4-chlorophenyl)-3-(3-cyanophenyl)-2-butanol (1.0 kg, 3.5 mol) in toluene (10 L) at 0° C. was added triethylamine (684 mL, 4.9 mol) and methanesulfonyl chloride (353 mL, 4.6 mol). After stirring for 5 min, the reaction mixture was filtered, and the precipitate was washed with toluene (8 L). The filtrate was washed with sodium bicarbonate (6 L, 50% saturated aqueous solution) and water (3 L), and concentrated to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07754188B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-74f6c06eb2874798b603a37031b3ba0b |
| Source note | uspto-grants-2010_07 |