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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1590375생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1590375

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물AnilineHCID 6115—
반응물NitroneHCID 6350—
반응물Sodium SulfiteHCID 24437—
반응물4-Chloro-3-(trifluoromethyl)anilineHCID 67574—
반응물Sodium AcetateHCID 517045—
반응물Formaldehyde, oxime, hydrochloride (1:1)HCID 20257314—
반응물Sodium NitriteHCID 23668193—
용매WaterHCID 962—
생성물4-Chloro-3-(trifluoromethyl)benzaldehydeHCID 1186428.8%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05202356
출처 데이터셋uspto-grants-1993_04
ORD IDord-32d3f09eb68347d3a7734a4a7956c177
출처 메모uspto-grants-1993_04