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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907006Generated: October 30, 2026

Trimethylamine → 1,1-Dimethoxy-1-(6-methoxy-2-naphthyl)prop-2-yl methanesulfonate

https://huagongshe.com/reaction/1907006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylamineHCID 1146—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant1,1-Dimethoxy-1-(6-methoxy-2-naphthyl)propan-2-olHCID 11300347—
SolventDichloromethaneHCID 6344—
Product1,1-Dimethoxy-1-(6-methoxy-2-naphthyl)prop-2-yl methanesulfonateHCID 12756330—

Reaction Conditions

Temperature10 °C

Reaction Steps

The crude oil, 1,1-dimethoxy-1-(6-methoxy-2-naphthyl)propan-2-ol, from Example 5 is dissolved in 250 ml of methylene chloride and cooled to 10° C. Then 12.2 g of trimethylamine is added and the reaction mixture is cooled to about 5° C. Over a 15 minute period, 10.55 g of methanesulfonyl chloride is added. The reaction mixture is stirred for about 30 minutes at 0°-5° C. Separation of the triethylamine hydrochloride as a precipitate is observed. The reaction mixture then is poured into 200 ml of water and extracted with methylene chloride. The organic phase is separated, dried over magnesium sulfate and evaporated under reduced pressure to yield 1,1-dimethoxy-1-(6-methoxy-2-naphthyl)prop-2-yl methanesulfonate as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04654438
Source datasetuspto-grants-1987_03
ORD IDord-90f530cbead24e158d98b3855819324e
Source noteuspto-grants-1987_03