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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22993Generated: October 25, 2026

Dichloromethane → 3-Bromo-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-1-ol

https://huagongshe.com/reaction/22993

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant3-BromophenolHCID 11563—
ReactantAmmonium ChlorideHCID 25517—
ReactantHexane, 2,5-dichloro-2,5-dimethyl-HCID 80360—
SolventWaterHCID 962—
Product3-Bromo-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-1-olHCID 22345465—

Reaction Steps

13.40 g (100.0 mmol) of ammonium chloride and 100 ml of dichloromethane are introduced into a three-necked flask under an argon atmosphere. A solution composed of 34.60 g (199.0 mmol) of 3-bromophenol, 89.00 g (486.0 mmol) of 2,5-dichloro-2,5-dimethylhexane and 300 ml of dichloromethane is added dropwise. The reaction mixture is stirred for sixteen hours at room temperature. The reaction mixture is poured into water and extracted with dichloromethane, the extract is washed with water and the organic phase is separated by settling, dried over magnesium sulphate and evaporated. The residue obtained is purified by chromatography on a silica column eluted with a mixture composed of 80% heptane and 20% dichloromethane. After evaporating the solvents, 30.00 g (53%) of the expected compound are collected in the form of white crystals with a melting point of 93° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06849658B2
Source datasetuspto-grants-2005_02
ORD IDord-99e55126c38b44819539451eb4d235a6
Source noteuspto-grants-2005_02