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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1799652Generated: October 30, 2026

2-Phenylethanol → HCID 66875136, compound

https://huagongshe.com/reaction/1799652

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PhenylethanolHCID 6054—
ReactantSodium hydrideHCID 24758—
Reactant9-Tetrahydropyranyloxy-1-bromononaneHCID 10946729—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66875136HCID 6687513639%

Reaction Steps

Sodium hydride (60% dispersion in mineral oil, 264 mg, 6.6 mmol) was added at 0° C. to a solution of 2-phenylethanol (807 mg, 6.61 mmol) in tetrahydrofuran (8.6 mL) and N,N-dimethylformamide (3.4 mL), then after 1 h a solution of 2-(9-bromo-nonyloxy)-tetrahydro-pyran (2.44 g, 7.93 mmol) in N,N-dimethylformamide (1.5 mL) was added dropwise. The solution was allowed to reach room temperature over 16 h, then partitioned between water and ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate, filtered, and evaporated. Chromatography (SiO2; heptane-ethyl acetate gradient) produced 2-(9-phenethyloxy-nonyloxy)-tetrahydro-pyran (898 mg, 39%). Colorless oil, m/e=366.2 ([M+NH4]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344027B2
Source datasetuspto-grants-2013_01
ORD IDord-60e7ad4602dc4ed2bb4fd615dd19f689
Source noteuspto-grants-2013_01