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HRID 343281作成日:2026年10月26日

Formaldehyde → 4-Ethyl-2-hydroxybenzaldehyde

https://huagongshe.com/reaction/343281

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物3-EthylphenolHCID 12101—
反応物HexamethylphosphoramideHCID 12679—
反応物HCID 178418443HCID 178418443—
溶媒TolueneHCID 1140—
溶媒TetrahydrofuranHCID 8028—
生成物4-Ethyl-2-hydroxybenzaldehydeHCID 1023601769.1%

反応手順

A stirred solution of 200 mL (0.20 mole) of 1.0M of ethylmagnesium bromide (in tetrahydrofuran) in 100 mL of tetrahydrofuran was cooled in an ice-bath and 25.0 grams (0.21 mole) of 3-ethylphenol was added dropwise. Upon completion of addition, the reaction mixture was allowed to warm to ambient temperature where it stirred for 30 minutes. After this time, 15.4 grams (0.51 mole) of paraformaldehyde, 36.7 grams (0.21 mole) of hexamethylphosphoramide, and 350 mL of toluene were added. Upon completion of addition, the reaction mixture was heated to 80° C. where it stirred for about 18 hours. The reaction mixture was then cooled and concentrated under reduced pressure to a residue. The residue was taken up in diethyl ether and 200 mL of an aqueous 10% hydrochloric acid solution was added. The aqueous layer was separated and extracted with diethyl ether. The extract was combined with the organic layer, and the combination was washed with water. The organic layer was dried with magnesium sulfate and filtered. The filtrate was concentrated under reduce pressure to a residue. The residue was subjected to column chromatography on silica gel, using 1:1 hexane and methylene chloride as the eluant. The product-containing fractions were combined and concentrated under reduced pressure, yielding 21.8 grams of 5-ethyl-2-formylphenol. The NMR spectrum was consistent with the proposed structure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05861359
出典データセットuspto-grants-1999_01
ORD IDord-b707ed1977ce42ceb5dcd42e9d14fa47
出典メモuspto-grants-1999_01