Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 861795Generated: October 30, 2026

Dichloromethane → 3-Bromo-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-ol

https://huagongshe.com/reaction/861795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant2-BromophenolHCID 7244—
ReactantHexane, 2,5-dichloro-2,5-dimethyl-HCID 80360—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventWaterHCID 962—
Product3-Bromo-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-olHCID 10779311—

Reaction Steps

36.6 g (0.2 mol) of 2,5-dichloro-2,5-dimethylhexane, 34.6 g (0.2 mol) of 2-bromophenol and 400 ml of dichloromethane were introduced successively into a three-necked flask. 26.6 g (0.2 mol) of AlCl3 were added in small amounts at 0° C. and stirring was carried out until gas evolution had ceased (violent reaction). The reaction mixture was poured into water and the organic phase was separated by settling, washed with an aqueous sodium bicarbonate solution, dried over magnesium sulfate and evaporated. The residue was purified by chromatography on a silica column eluted with a mixture of ethyl acetate and heptane (10/90). After evaporating the solvents, 20.6 g (36%) of the expected phenol were recovered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05716624
Source datasetuspto-grants-1998_02
ORD IDord-bcf77d8ef8a1431a8181af36e3c0aeab
Source noteuspto-grants-1998_02