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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252158Generated: October 26, 2026

Boron trifluoride etherate → 6-Methoxy-1-benzothiophene

https://huagongshe.com/reaction/252158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluoride etherateHCID 8000—
ReactantSodium BicarbonateHCID 516892—
Reactant(3-Methoxyphenylsulphanyl)acetaldehydeHCID 13642522—
SolventDichloromethaneHCID 6344—
Product6-Methoxy-1-benzothiopheneHCID 1363423761%

Reaction Conditions

Temperature0 °C

Reaction Steps

Boron trifluoride etherate (8.15 mL) dissolved in dry dichloromethane (407 mL) was stirred rapidly at 0° C. under nitrogen and a solution of (3-methoxyphenylsulphanyl)acetaldehyde (11.5 g, 63.10 mmol) in dry dichloromethane (29 mL) was added dropwise over 25 min. The resultant green solution was stirred for 2 min and then saturated aqueous sodium bicarbonate solution (150 mL) was added at a rate so as to maintain the temperature <8° C. The reaction mixture was stirred for 5 min and then the layers were separated and the organic layer was washed with saturated aqueous sodium bicarbonate solution (100 mL) and water (100 mL). The organic phase was dried (MgSO4), and concentrated in vacuo. The product was purified by distillation to afford the title compound as a colourless oil (6.29 g, 61%, b.p. 83-88° C. at 16 mBar).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868017B2
Source datasetuspto-grants-2011_01
ORD IDord-b895cfdf07434aa0b96cdc991f555e2b
Source noteuspto-grants-2011_01