戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1935作成日:2026年10月24日

Hydrogen Peroxide → 2-(4-Pentynyloxy)tetrahydro-2H-pyran

https://huagongshe.com/ja/reaction/1935

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen PeroxideHCID 784—
反応物4-Toluenesulfonyl chlorideHCID 7397—
反応物3,4-dihydro-2H-pyranHCID 8080—
反応物TriphenylphosphineHCID 11776—
反応物BromineHCID 24408—
反応物Hydrazine hydrate (1:1)HCID 24654—
反応物Lithium aluminum hydrideHCID 28112—
反応物2-(3-Butynyloxy)tetrahydro-2H-pyranHCID 142440—
反応物ButyllithiumHCID 178418339—
触媒Silver NitrateHCID 24470—
生成物2-(4-Pentynyloxy)tetrahydro-2H-pyranHCID 357816—

反応手順

Hydrazine hydrate and hydrogen peroxide (30 wt. % solution in water) were purchased from Mallinckrodt (Chesterfield, Mo.) and Fisher Chemical Co. (Fair Lawn, N.J.), respectively. Butyllithium (1.6M and 2.5M solutions in hexane), 2-(3-butynyloxy)tetrahydro-2H-pyran (1-(tetrahydopyran-2-yloxy)-3-butyne), lithium tetrahydridoaluminate, borane-methylsulfide complex, Cu(I)Br.Me2S complex, and p-toluenesulfonyl chloride from Aldrich Chemical Co. (Milwaukee, Wis.), and bromine and triphenylphosphine from Fluka Chemical Co. (Ronkonkoma, N.Y.), were used as purchased. 1-(Tetrahydopyran-2-yloxy)-4-pentyne was prepared from the corresponding alcohol using the methods described in Robertson, "Adducts of tert-alcohols containing an ethynyl group with dihydropyran. Potentially useful intermediates," J. Org. Chem. 25:931-932 (1960), the disclosure of which is hereby incorporated by reference. Column chromatography was run on silica gel (Merck, H 60), and reactions were monitored by TLC on Baker-flex Silica gel IB2-F plates (J. T. Baker). Silver nitrate column chromatography was done on silica gel impregnated with AgNO3 (20% of AgNO3 on silica gel Merck H 60).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05728376
出典データセットuspto-grants-1998_03
ORD IDord-da3a70b3badd4e8da28a4299f8a4a21a
出典メモuspto-grants-1998_03