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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403466Generated: November 1, 2026

Benzaldehyde → 1-phenyl-4-(tetrahydro-2H-pyran-2-yloxy)but-2-yn-1-ol

https://huagongshe.com/reaction/1403466

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantTetrahydro-2-(2-propynyloxy)-2H-pyranHCID 98609—
ReactantSodium BicarbonateHCID 516892—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1-phenyl-4-(tetrahydro-2H-pyran-2-yloxy)but-2-yn-1-olHCID 70665277—

Reaction Conditions

Temperature-30 °C

Reaction Steps

To a solution of 2-(prop-2-ynyloxy)-tetrahydro-2H-pyran (10.0 g, 71.4 mmol) in THF (40 mL) was added n-BuLi (2.5M, 31.4 mL, 78.6 mmol) at −78° C. The reaction mixture was kept for 1 h at −78° C. and then benzaldehyde (8.3 g, 78.6 mmol) was added at −78° C. The reaction mixture was stirred for 2 h and then slowly warmed to −30° C. before being poured into NaHCO3 (aq., 500 mL), extracted with ethyl acetate (3×200 mL), dried over anhydrous sodium sulfate and then concentrated in vacuo to afford 1-phenyl-4-(tetrahydro-2H-pyran-2-yloxy)but-2-yn-1-ol as a colorless oil (17.0 g, crude).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912188B2
Source datasetuspto-grants-2014_12
ORD IDord-8404a5a4071745c2a48ceb630f6f0e9b
Source noteuspto-grants-2014_12