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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2185162Generated: October 29, 2026

Acetylene → 6-Cyclopentylidene-3-methylhex-1-yn-3-ol

https://huagongshe.com/reaction/2185162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetyleneHCID 6326—
Reactant5-Cyclopentylidenepentan-2-oneHCID 13528013—
ReactantHCID 178418922HCID 178418922—
SolventTetrahydrofuranHCID 8028—
Product6-Cyclopentylidene-3-methylhex-1-yn-3-olHCID 1843385281%

Reaction Steps

Acetylene was bubbled for 50 minutes through a solution of tBuOK (33.8 g; 0.30 mol) in THF (240 ml) at 0° C. The resulting beige suspension was treated with 5-cyclopentylidenepentan-2-one (41.7 g; 0.27 mol) added dropwise for 15 minutes at 0° C. The resulting mixture was warmed gently to room temperature and quenched with saturated NH4Cl (180 ml). The aqueous phase was separated and extracted with MTBE (2×120 ml). The combined organic layers were washed with H2O (240 ml), brine (100 ml), dried over MgSO4, and concentrated in vacuo. Distillation (69° C.-71° C./0.09 torr) afforded 38.95 g (81% yield) of 6-cyclopentylidene-3-methylhex-1-yn-3-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06399811B1
Source datasetuspto-grants-2002_06
ORD IDord-d457b3ff82a24073bb695f55caf34eed
Source noteuspto-grants-2002_06