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HRID 570296作成日:2026年10月26日

Isopropanol → 2-(benzyloxymethyl)-3,4-dihydro-2H-pyran

https://huagongshe.com/reaction/570296

反応式

関与物質

役割名称HCID仕込み量
反応物IsopropanolHCID 3776—
反応物Sodium HydroxideHCID 14798—
反応物((2-(Allyloxy)pent-4-enyloxy)methyl)benzeneHCID 12996273—
触媒Benzylidenebis(tricyclohexylphosphine)dichlororutheniumHCID 11967259—
溶媒TolueneHCID 1140—
生成物2-(benzyloxymethyl)-3,4-dihydro-2H-pyranHCID 4095658—

反応条件

温度120 °C

反応手順

Benzylidene-bis(tricyclohexylphosphine)dichlororuthenium, bis(tricyclohexylphosphine)benzylidine ruthenium(IV) chloride-Grubbs 1 generation catalyst (0.5 g, 0.54 mmol) was added in one portion to a stirred solution of ((2-(allyloxy)pent-4-enyloxy)methyl)benzene (12) (4 g, 17.2 mmol) in toluene (200 mL). The resulting mixture was heated at 50° C. under N2 for 2 hours before isopropanol (18 mL) and NaOH (0.17 g) were added. The mixture was then heated at 120° C. overnight. The solvent was evaporated and the residue was purified over silica gel using Et2O and hexane to give 2-(benzyloxymethyl)-3,4-dihydro-2H-pyran (13).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09023839B2
出典データセットuspto-grants-2015_05
ORD IDord-3f0ccf4746014d68b9ce7d101071b31f
出典メモuspto-grants-2015_05