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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2106737Generated: October 31, 2026

Hydrochloric Acid → 1-(4,4,7,7-Tetramethyl-4,5,6,7-tetrahydro-1-benzothiophen-2-yl)ethan-1-one

https://huagongshe.com/reaction/2106737

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetyl chlorideHCID 6367—
ReactantTin tetrachlorideHCID 24287—
Reactant4,4,7,7-Tetramethyl-4,5,6,7-tetrahydro-1-benzothiopheneHCID 18466851—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
Product1-(4,4,7,7-Tetramethyl-4,5,6,7-tetrahydro-1-benzothiophen-2-yl)ethan-1-oneHCID 2304923398%

Reaction Conditions

Temperature0 °C

Reaction Steps

18.2 g of 4,5,6,7-tetrahydro-4,4,7,7-tetramethylbenzo[b]thiophene and 7.4 g of acetyl chloride are dissolved in 200 ml of benzene and the solution is cooled to 0° C. At this temperature there are slowly added dropwise thereto 24.4 g of tin tetrachloride. After stirring at room temperature for 2.5 hours, the mixture is again cooled to 0° C. and a mixture of 9.3 ml of concentrated hydrochloric acid and 36.4 ml of water is added dropwise thereto. The mixture is extracted with ether, the organic phase is washed once with water, dried, evaporated and distilled in a high vacuum. There are obtained 21.7 g of 2-acetyl-4,5,6,7-tetrahydro-4,4,7,7-tetramethylbenzo[b]thiophene as a colorless liquid, b.p. 108°-115° C./0.05 mm, which can be crystallized from hexane, m.p. 53°-55° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04931458
Source datasetuspto-grants-1990_06
ORD IDord-8c2f5c41b349406fb741da74058c8119
Source noteuspto-grants-1990_06