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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703104Generated: November 1, 2026

Triethylamine → 6-Phenylhex-1-yl methylsulfonate

https://huagongshe.com/reaction/1703104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant6-Phenyl-1-hexanolHCID 520110—
SolventDichloromethaneHCID 6344—
Product6-Phenylhex-1-yl methylsulfonateHCID 13079702—

Reaction Conditions

Temperature-4 °C

Reaction Steps

To a chilled (-4° C.) solution of 19.4 g. of 6-phenylhexanol (prepared as described in Example 46) and 15.1 g. of triethylamine in 500 ml. of dichloromethane is added dropwise, over 5 minutes, 12.6 g. of methanesulfonyl chloride. The mixture is stirred at -10° C. for 30 minutes and the solution washed successively with 200 ml. of cold water, 200 ml. of cold 10% hydrochloric acid, 200 ml. of cold saturated sodium bicarbonate and 200 ml. of cold saturated sodium chloride solution. The organic layer is dried over magnesium sulfate and the solvent removed under reduced pressure to give 6-phenylhexanol O-methanesulfonate as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04350822
Source datasetuspto-grants-1982_09
ORD IDord-8858bfde2c0d4132bcecb9ac31a9c0a0
Source noteuspto-grants-1982_09