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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251708Generated: November 2, 2026

Tetrahydrofuran → Thiophene, 2-(phenylmethyl)-

https://huagongshe.com/reaction/1251708

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 numberUS06342610B2
Source datasetuspto-grants-2002_01
ORD IDord-80d2258890294630b6c2c37970a7a821
Source noteuspto-grants-2002_01