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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2194881Generated: November 1, 2026

Methanesulfonyl chloride → (2'-Chloro-3-methylbiphenyl-4-yl)methyl methanesulfonate

https://huagongshe.com/reaction/2194881

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
Reactant(2'-Chloro-3-methylbiphenyl-4-yl)methanolHCID 67448566—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product(2'-Chloro-3-methylbiphenyl-4-yl)methyl methanesulfonateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08334308B2
Source datasetuspto-grants-2012_12
ORD IDord-4e3be230bca0449c922820128be7d0df
Source noteuspto-grants-2012_12