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HRID 254855作成日:2026年10月26日

Acetone → 4-(2,3-Dihydroxypropoxy)benzaldehyde

https://huagongshe.com/reaction/254855

反応式

関与物質

役割名称HCID仕込み量
反応物AcetoneHCID 180—
反応物Methyl morpholine oxideHCID 82029—
反応物4-(Allyloxy)benzaldehydeHCID 95942—
触媒Osmium TetroxideHCID 30318—
溶媒WaterHCID 962—
溶媒tert-ButanolHCID 6386—
溶媒Ethyl AcetateHCID 8857—
生成物4-(2,3-Dihydroxypropoxy)benzaldehydeHCID 16655848—

反応手順

To a solution of 4-allyloxybenzaldehyde (1.0 g, 6.17 mmol) in acetone (40 mL) and water (5 mL) is added a 2.5% solution of OsO4 in tert. butanol (1.25 mL) followed by N-methyl morpholine-N-oxide (867 mg, 7.4 mmol). The pale yellow solution is stirred at it for 6 h, diluted with EA (250 mL) and washed with 10% aq. citric acid solution (100 mL) and water (2×100 mL). The washings are extracted with EA (150 mL). The combined organic extracts are concentrated and purified by column chromatography on silica gel to give the title compound (731 mg) as a turbid oil. The title compound reversibly polymerizes upon standing. LC-MS: tR=0.58 min, [M+1+CH3CN]+=238.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07875726B2
出典データセットuspto-grants-2011_01
ORD IDord-c7cd5571193440c9b7466399a660232c
出典メモuspto-grants-2011_01