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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739103Generated: November 1, 2026

Bromine → 5,6,7,8-Tetrahydro-5,5,8,8-tetramethyl-1-bromo-2-hydroxynaphthalene-3-carboxylic acid

https://huagongshe.com/reaction/1739103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant3-Hydroxy-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalene-2-carboxylic acidHCID 10682016—
Product5,6,7,8-Tetrahydro-5,5,8,8-tetramethyl-1-bromo-2-hydroxynaphthalene-3-carboxylic acidHCID 10639884—

Reaction Steps

3-Hydroxy-5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl acid (Compound L, 155 mg, 0.62 mmol) was dissolved in 1 ml of HOAC. To this solution was added Br2 (0.033 ml, 0.62 mmol). The reaction mixture was left at room temperature for over night. A stream of air was passed through the reaction mixture to remove the unreacted Br2. The remaining solid was dissolved in small amount of THF and purified by column chromatography (ethyl acetate/hexane 1/1) to yield the desired product as a cream colored solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05965606
Source datasetuspto-grants-1999_10
ORD IDord-2fcdb4f94c354550b00895320396ecd3
Source noteuspto-grants-1999_10