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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485919Generated: October 26, 2026

Acetaldehyde → 6,7-Dichloro-5-hydroxy-alpha-methylbenzo[b]thiophene-2-methanol

https://huagongshe.com/reaction/485919

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantHydrochloric AcidHCID 313—
Reactant6,7-Dichloro-1-benzothiophene-5-olHCID 13289997—
ReactantCarbontetrachloride dry-iceHCID 86602444—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product6,7-Dichloro-5-hydroxy-alpha-methylbenzo[b]thiophene-2-methanolHCID 13477654—

Reaction Steps

To a solution of 25 g of 6,7-dichloro-5-hydroxybenzo[b]thiophene in 145 ml of dried tetrahydrofuran at -25° to -30° is added 110 ml of 2.5M n-butyllithium maintaining a temperature below -21°. After the addition, the carbon tetrachloride-dry ice bath is replaced with an ice-water bath and the mixture is stirred at 0°-5° for 4 hrs. A solution of 7.5 ml of freshly distilled acetaldehyde in 10 ml tetrahydrofuran is added dropwise. An additional 2 ml of acetaldehyde is added and the solution is stirred for 1 hr. The solution is poured onto 500 ml of a cold 5% hydrochloric acid solution and the mixture is extracted with ethyl ether. The ether extracts are washed, dried over anhydrous magnesium sulfate, filtered and solvent is removed to give a solid. Recrystallization from ethyl acetate and hexane gives 20 g of 6,7-dichloro-5-hydroxy-α-methylbenzo[b]thiophene-2-methanol, mp 173°-174°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04537976
Source datasetuspto-grants-1985_08
ORD IDord-1d1fde232b8843a4b2aeeb6b7ae7ff7f
Source noteuspto-grants-1985_08