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HRID 6435作成日:2026年10月23日

Phenol → (2,2-Diethoxyethoxy)benzene

https://huagongshe.com/ja/reaction/6435

反応式

関与物質

役割名称HCID仕込み量
反応物PhenolHCID 996—
反応物Sodium hydrideHCID 24758—
反応物Ethane, 2-bromo-1,1-diethoxy-HCID 74852—
溶媒2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
生成物(2,2-Diethoxyethoxy)benzeneHCID 96328—

反応条件

温度110 °C

反応手順

Sodium hydride (5.83 g of a 55% dispersion in mineral oil) was added to a solution of phenol (12.56 g) in DMPU (25 ml) at 5° C. and the mixture was stirred for 30 minutes. Bromoacetaldehyde diethyl acetal (10.05 ml) was added and the mixture was heated at 110° C. for 5 hours, then allowed to cool. The mixture was partitioned between ethyl acetate (100 ml) and water (100 ml) and the organic phase was separated and washed sequentially with aqueous 2M sodium hydroxide solution (2×50 ml) and water (50 ml). The aqueous fractions were combined and re-extracted with ethyl acetate (100 ml). The combined organic extracts were dried (MgSO4) and concentrated. The resultant oil was purified by flash column chromatography, eluting with ethyl acetate/hexane (1:10 v/v) to give 2-phenoxyacetaldehyde diethyl acetal (9.43 g) as an oil; NMR: 1.25(6H,t, J=7.0 Hz), 3.6-3.85(4H,m), 4.05(2 H,d, J=6.0 Hz), 4.85 (1H,t, J=6.0 Hz) and 6.9-7.35(5H,m).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05248780
出典データセットuspto-grants-1993_09
ORD IDord-db8a01301d8543ea840e78a021d649d8
出典メモuspto-grants-1993_09