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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477007Generated: October 25, 2026

Hexane → 1-Phenyl-8-(2-tetrahydropyranyloxy)-1-octyne

https://huagongshe.com/reaction/477007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantPhenylacetyleneHCID 10821—
Reactant2-[(6-bromohexyl)oxy]tetrahydro-2H-pyranHCID 103860—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexamethylphosphoramideHCID 12679—
Product1-Phenyl-8-(2-tetrahydropyranyloxy)-1-octyneHCID 1483422058.3%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a solution of 11.2 g of phenylacetylene dissolved in 100 ml of tetrahydrofuran, 78.8 ml of 1.6M-hexane solution of n-butyl lithium was added dropwise at 5°-8° C. Then 150 ml of a hexamethylphosphoramide solution containing 29.4 g of 1-bromo-6-(2-tetrahydropyranyloxy)-hexane was added dropwise at 10°-20° C. After stirring at 20° C. for 30 minutes, the reaction mixture was poured into ice-water and extracted with hexane. The organic layer was washed with water, dried and then the organic solvent was distilled off. The residue was purified by silica gel column chromatography (solvent: hexane-ethyl acetate=10:1), to give 18.3 g of 1-phenyl-8-(2-tetrahydropyranyloxy)-1-octyne as an oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04886817
Source datasetuspto-grants-1989_12
ORD IDord-5198d37285e94e4c917601bdb7bb3bf0
Source noteuspto-grants-1989_12