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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943162Generated: November 1, 2026

Tetrahydrofuran → 6,7-dihydro-5H-cyclopenta[c]pyridin-3-ylmethanol

https://huagongshe.com/reaction/1943162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 6,7-dihydro-5H-cyclopenta[c]pyridine-3-carboxylateHCID 14735905—
ReactantAluminium lithium hydrideHCID 21226445—
SolventWaterHCID 962—
Product6,7-dihydro-5H-cyclopenta[c]pyridin-3-ylmethanolHCID 6859818857%

Reaction Steps

A solution of ethyl 6,7-dihydro-5H-cyclopenta[c]pyridine-3-carboxylate (427 mg, 2.233 mmol) in (THF) (20 ml) at −78° C. under argon was treated with LiAlH4 (1M in THF) (2.233 ml, 2.233 mmol) and allowed warm to rt. After 10 min at rt, water (1 ml), 2M aq NaOH (1 ml) and water (1 ml) were sequentially added and the mixture stirred at rt for 0.5 h. The mixture was then filtered through a short pad of Kieselguhr, eluting with THF (50 ml), organic extracts were then evaporated, chromatographed (0-20% methanol/DCM) to give product as an orange oil (189 mg, 57%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389524B2
Source datasetuspto-grants-2013_03
ORD IDord-f29bbf7464454e999db688c28c5c919f
Source noteuspto-grants-2013_03