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HRID 1590375作成日:2026年10月26日

Hydrochloric Acid → 4-Chloro-3-(trifluoromethyl)benzaldehyde

https://huagongshe.com/reaction/1590375

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物AnilineHCID 6115—
反応物NitroneHCID 6350—
反応物Sodium SulfiteHCID 24437—
反応物4-Chloro-3-(trifluoromethyl)anilineHCID 67574—
反応物Sodium AcetateHCID 517045—
反応物Formaldehyde, oxime, hydrochloride (1:1)HCID 20257314—
反応物Sodium NitriteHCID 23668193—
溶媒WaterHCID 962—
生成物4-Chloro-3-(trifluoromethyl)benzaldehydeHCID 1186428.8%

反応手順

To a suspension of 4-chloro-3-trifluoromethylaniline (ex Fluorochem) (15.9 g) in water (16 ml) was added concentrated hydrochloric acid (18 ml) Ice (30 g) was added and the mixture cooled to 0° and treated with sodium nitrite (5.6 g) in water (8 ml). After 15 minutes the mixture was made neutral to congo red with sodium acetate (8 g) in water (10 ml). A solution of formaldoxime, prepared from formaldoxime hydrochloride (ex Lancaster) (9.9 g) and sodium acetate (12 g) (ex BDH) in water (57 ml), at 10° was treated with cupric sulphate (2 g) (ex BDH) and sodium sulphite (0.34 g) followed by sodium acetate (55 g) in water (60 ml). The previously prepared mixture (from the aniline) was added dropwise at 10°-15°. After one hour at 15° hydrochloric acid (77 ml) was added and the mixture worked up in the usual manner. Purification by distillation (80°, 0.5 mmHg) gave 4-chloro-3-trifluoromethylbenzaldehyde (1.5 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05202356
出典データセットuspto-grants-1993_04
ORD IDord-32d3f09eb68347d3a7734a4a7956c177
出典メモuspto-grants-1993_04