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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234360Generated: October 31, 2026

Tetrahydrofuran → Thiophene, 2-(phenylmethyl)-

https://huagongshe.com/reaction/234360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 69948862HCID 69948862—
ProductThiophene, 2-(phenylmethyl)-HCID 13939168%

Reaction Steps

A solution of 1-(2-thienyl)benzyl acetate in THF (5 ml) was added carefully to dry liquid ammonia (100 ml). Lithium metal was added in small portions until the blue color persisted. The resulting reaction mixture was stirred for 30 min, and the reaction was quenched by addition of solid ammonium chloride. The residue, after complete evaporation of liquid ammonia, was dissolved in water (50 ml) and was extracted with methylene chloride (2×50 ml). The combined organic layers was dried over MgSO4 and filtered. Removal of the solvent gave crude product, which was purified by column chromatography using hexane as eluent to give 2-benzylthiophene (1.2 g, 68% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05594021
Source datasetuspto-grants-1997_01
ORD IDord-6e4b080555944b6086ec808b0b21ee1b
Source noteuspto-grants-1997_01