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HRID 38717作成日:2026年10月25日

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

https://huagongshe.com/reaction/38717

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 rt 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US08524752B2
出典データセットuspto-grants-2013_09
ORD IDord-0e52fbecea614b5dbc1e4621228d68ef
出典メモuspto-grants-2013_09