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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206736Generated: November 1, 2026

Trifluoroacetic acid → 2,3-Dihydrobenzo(b)thiophene

https://huagongshe.com/reaction/2206736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantBenzo(B)ThiopheneHCID 7221—
ReactantTriethylsilaneHCID 12052—
Product2,3-Dihydrobenzo(b)thiopheneHCID 7831941%

Reaction Conditions

Temperature50 °C

Reaction Steps

Trifluoroacetic acid (5.2 mL) was slowly added to the mixture of benzothiophene (1 g, 7.45 mmol) and triethylsilane (3.6 mL, 22.35 mmol) with heating under reflux at 50° C. for 125 hours. After cooling to 0° C., the reaction was quenched by addition of aq. saturated NH4Cl solution. The mixture was diluted with water and extracted with EtOAc. The organic layer was washed with brine, dried over anhydrous MgSO4, filtered and evaporated in vacuo. The residue was purified by silica gel column chromatography to provide the intermediate 112 (415 mg, 41%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371303B2
Source datasetuspto-grants-2016_06
ORD IDord-3078f579ce5f4bb3a684c76de2db17d8
Source noteuspto-grants-2016_06