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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1030808Generated: November 2, 2026

2-Chloroethyl methyl sulfide → methyl 2-[p-[(E)-2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-propenyl]phenoxy]ethyl sulphide

https://huagongshe.com/reaction/1030808

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloroethyl methyl sulfideHCID 10965—
ReactantPotassium CarbonateHCID 11430—
ReactantRo 14-6113HCID 6439236—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Productmethyl 2-[p-[(E)-2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-propenyl]phenoxy]ethyl sulphideHCID 6778664574.4%

Reaction Steps

A mixture of 6 g of p-[(E)-2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)propenyl]phenol, 4.8 g of 2-chloroethyl methyl sulphide and 10.5 g finely powdered potassium carbonate in 100 ml of dimethylformamide is heated to 100° for 20 hours. The cooled reaction mixture is diluted with water and extracted several times with ethyl acetate. The crystalline residue obtained after drying and evaporating the organic phase is recrystallized from hexane and gives 5.5 g of methyl 2-[p-[(E)-2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-propenyl]phenoxy]ethyl sulphide in colourless crystals, melting point 94°-96°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05106981
Source datasetuspto-grants-1992_04
ORD IDord-65482cdbd37140a2998b05fd11bbcf4a
Source noteuspto-grants-1992_04