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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903489Generated: October 26, 2026

Acetone → 6,7-Dichloro-5-hydroxy-alpha,alpha-dimethylbenzo[b]thiophene-2-methanol

https://huagongshe.com/reaction/1903489

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
Reactant6,7-Dichloro-1-benzothiophene-5-olHCID 13289997—
ReactantCarbontetrachloride dry-iceHCID 86602444—
ReactantButyllithiumHCID 178418339—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product6,7-Dichloro-5-hydroxy-alpha,alpha-dimethylbenzo[b]thiophene-2-methanolHCID 13290042—

Reaction Steps

To a solution of 6,7-dichloro-5-hydroxybenzo[b]thiophene in 28 ml of dried tetrahydrofuran at -28° is added 21 ml of 2.5 M n-butyllithium, maintaining the temperature below -18°. Following the addition, the carbon tetrachloride-dry ice bath is replaced with an ice-water bath and the mixture is stirred at 0°-5° for about 4 hrs. A solution of 3.3 ml of acetone in 10 ml tetrahydrofuran is added dropwise. After stirring for one hr, the solution is poured onto 100 ml of water and acidified to pH=5-6 with glacial acetic acid. The acidic solution is extracted with ethyl acetate, washed, dried over anhydrous magnesium sulfate, filtered and the solvent is removed to give 3.84 g of 6,7-dichloro-5-hydroxy-α,α-dimethylbenzo[b]thiophene-2-methanol, mp 171°-173°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04436748
Source datasetuspto-grants-1984_03
ORD IDord-097b3b01fb4c4e98b125c9314a8b52ec
Source noteuspto-grants-1984_03