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HRID 477007作成日:2026年10月26日

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

https://huagongshe.com/reaction/477007

反応式

関与物質

役割名称HCID仕込み量
反応物HexaneHCID 8058—
反応物PhenylacetyleneHCID 10821—
反応物2-[(6-bromohexyl)oxy]tetrahydro-2H-pyranHCID 103860—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexamethylphosphoramideHCID 12679—
生成物1-Phenyl-8-(2-tetrahydropyranyloxy)-1-octyneHCID 1483422058.3%

反応条件

温度20 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04886817
出典データセットuspto-grants-1989_12
ORD IDord-5198d37285e94e4c917601bdb7bb3bf0
出典メモuspto-grants-1989_12