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HRID 372266作成日:2026年10月27日

2-[(6-bromohexyl)oxy]tetrahydro-2H-pyran → 1-(6-Tetrahydropyranyloxyhexyl)-1-hydroxymethylcyclopent-3-ene

https://huagongshe.com/reaction/372266

反応式

関与物質

役割名称HCID仕込み量
反応物2-[(6-bromohexyl)oxy]tetrahydro-2H-pyranHCID 103860—
反応物Methyl cyclopent-3-ene-1-carboxylateHCID 1514118—
生成物1-(6-Tetrahydropyranyloxyhexyl)-1-hydroxymethylcyclopent-3-eneHCID 54021530—

反応手順

The above procedure was repeated except that methyl cyclopent-3-ene carboxylate (prepared as described by A. H. Schmid and A. W. Wolkoff, J. Org. Chem. 32, 254 (1967)) was used with the 6-tetrahydropyranyloxyhexyl bromide of part D of this example and 1-(6-tetrahydropyranyloxyhexyl)-1-hydroxymethylcyclopent-3-ene was obtained as an oil (IR 3400, 3010 cm-1, nmr τ 4.4, 5.4, 6.35, 7.8, 8.5).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04090019
出典データセットuspto-grants-1978_05
ORD IDord-5b7565c711c34383a61ba5d7a22531a1
出典メモuspto-grants-1978_05