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HRID 257355作成日:2026年10月26日

Formaldehyde → 4-Chloro-2-hydroxybenzaldehyde

https://huagongshe.com/reaction/257355

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-ChlorophenolHCID 7933—
反応物TetrahydrofuranHCID 8028—
反応物HexamethylphosphoramideHCID 12679—
反応物HCID 178418443HCID 178418443—
溶媒TolueneHCID 1140—
溶媒Diethyl EtherHCID 3283—
生成物4-Chloro-2-hydroxybenzaldehydeHCID 52010173.5%

反応条件

温度80 °C

反応手順

A 2M solution of ethylmagnesium bromide in tetrahydrofuran (50 ml, 0.10 mole) was placed in a flask, and a solution of 12.85 g (0.10 mole) of 3-chlorophenol in 50 mL of diethyl ether was added slowly with stirring. The addition required two hours, after which the solvents were removed by evaporation under reduced pressure. Toluene (200 ml), 7.50 g (0.25 mole) of paraformaldehyde, and 17.92 g (0.10 mole) of hexamethylphosphoramide were added to the residue, and this mixture was heated at 80° C. for approximately 16 hours. The solvent was evaporated under reduced pressure, leaving a residue. This residue was washed successively with 50 mL of hydrochloric acid and 300 mL of water. Vacuum distillation of the washed residue yielded 11.50 g of 4-chlorosalicylaldehyde, b.p. 112° C. at 9 mm of Hg. This reaction was repeated several times.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05262390
出典データセットuspto-grants-1993_11
ORD IDord-e8df0bebc4294be48db9951d1906c2d9
出典メモuspto-grants-1993_11