HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonyl chloride → (2'-Chloro-3-methylbiphenyl-4-yl)methyl methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (2'-Chloro-3-methylbiphenyl-4-yl)methanol | HCID 67448566 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (2'-Chloro-3-methylbiphenyl-4-yl)methyl methanesulfonate | HCID 86658848 | — |
Reaction Steps
To a solution of (2′-chloro-3-methylbiphenyl-4-yl)methanol from step 1 in CH2Cl2 (0.13M) at 0° C. was added diisopropyl ethylamine (1.5 eq.) then methanesulfonyl chloride (1.1 eq.). The reaction mixture was stirred at room temperature for 2 h, poured in water and extracted with EtOAc. The organic extract was washed with water, brine, dried over MgSO4 filtered and concentrated to afford the title compound which was used as such in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08334308B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-4e3be230bca0449c922820128be7d0df |
| Source note | uspto-grants-2012_12 |