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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058365Generated: October 31, 2026

Benzo(B)Thiophene → 1-Benzothiophene-3-carbaldehyde

https://huagongshe.com/reaction/1058365

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzo(B)ThiopheneHCID 7221—
ReactantButyl Dichloromethyl EtherHCID 4278354—
CatalystTitanium TetrachlorideHCID 24193—
SolventCarbon DisulfideHCID 6348—
Product1-Benzothiophene-3-carbaldehydeHCID 22732815.2%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of benzothiophene (1.08 g, 8.0 mmol) in carbon disulfide (20 mL) at 0° C. was added titanium tetrachloride (3 mL, 27.3 mmol) followed by dichloromethyl n-butyl ether (1.24 g, 7.9 mmol) slowly dropwise. The reaction mixture was warmed to 25° C. and stirred for 1.5 h. The reaction was quenched with conc. hydrochloric acid solution (1 mL), diluted with chloroform (60 mL) and washed with water (50 mL), saturated sodium bicarbonate solution (2×30 mL) and brine (30 mL). The organic layer was dried (MgSO4), filtered, concentrated and flash chromatographed (silica gel, 2.5-5% diethyl ether in petroleum ether) to afford benzothiophene-3-carboxaldehyde (195 mg, 15% yield) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06515124B2
Source datasetuspto-grants-2003_02
ORD IDord-d72e388e4ff94d02ad7a6da3d3f88ea1
Source noteuspto-grants-2003_02