Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655401Generated: October 31, 2026

m-Chloroperbenzoic acid → methyl 2-[p-[(E)-2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)propenyl]phenoxy]ethyl sulphoxide

https://huagongshe.com/reaction/1655401

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactantmethyl 2-[p-[(E)-2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)-propenyl]phenoxy]ethyl sulphideHCID 67786645—
SolventChloroformHCID 6212—
Productmethyl 2-[p-[(E)-2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)propenyl]phenoxy]ethyl sulphoxideHCID 6778592577.8%

Reaction Steps

2.1 g of the compound obtained in Example 5 are dissolved in 50 ml of chloroform and treated slowly at 0° with a solution of 1.2 g of m-chloroperbenzoic acid (90%) in 10 ml of chloroform. After stirring at 0° for 20 hours the mixture is washed with dilute soda solution and water, dried and evaporated. The thus-obtained yellow oil is filtered over a small silica gel column (eluting agent hexane/ethyl acetate=1:2) and recrystallized from ethyl acetate. There are obtained 1.7 g of methyl 2-[p-[(E)-2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthyl)propenyl]phenoxy]ethyl sulphoxide, melting point 134°-136°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05250562
Source datasetuspto-grants-1993_10
ORD IDord-5d5010c90702480e8c69e5bc9de4f048
Source noteuspto-grants-1993_10