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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106460Generated: October 31, 2026

Benzo(B)Thiophene → HCID 15550519, compound

https://huagongshe.com/reaction/1106460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzo(B)ThiopheneHCID 7221—
Reactant4,5-Dimethyl-2-furaldehydeHCID 643406—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15550519HCID 15550519102.2%

Reaction Steps

n-Butyl lithium (2.5 N in hexanes, 32.2 mL, 80.5 mmol) was added to a stirred solution of thianaphthene (10.6 g, 78.9 mmol) in THF (290 mL) at -78° C. After 15 min., a solution of 4,5-dimethyl-2-furaldehyde (9.79 g, 78.9 mmol) in THF (10 mL) was added. After additional 1 hour, the reaction mixture was quenched with 10% aqueous ammonium chloride (150 mL) and further diluted with water (150 mL). Aqueous mixture was extracted with dichloromethane. The combined dichloromethane extracts were washed with water, dried with brine and anhydrous Na2SO4, and concentrated to provide the title compound as an yellow oil (20.84 g, 100%): NMR (DMSO-d6); δ7.89 (d, J=8 Hz, 1H), 7.76 (d, J=8, Hz, 1H), 7.35-7.26 (m, 2H), 7.25 (s, 1H), 6.36 (s, 1H), 6.08 (s, 1H), 5.92 (s, 1H), 2.13 (s, 3H), 1.86 (s, 3H); MS (EI): [M+], 258.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06057316
Source datasetuspto-grants-2000_05
ORD IDord-6df915da9b83416a88208e0345b0ee1c
Source noteuspto-grants-2000_05