참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Aniline | HCID 6115 | — |
| 반응물 | Nitrone | HCID 6350 | — |
| 반응물 | Sodium Sulfite | HCID 24437 | — |
| 반응물 | 4-Chloro-3-(trifluoromethyl)aniline | HCID 67574 | — |
| 반응물 | Sodium Acetate | HCID 517045 | — |
| 반응물 | Formaldehyde, oxime, hydrochloride (1:1) | HCID 20257314 | — |
| 반응물 | Sodium Nitrite | HCID 23668193 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 4-Chloro-3-(trifluoromethyl)benzaldehyde | HCID 118642 | 8.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05202356 |
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| 출처 데이터셋 | uspto-grants-1993_04 |
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| ORD ID | ord-32d3f09eb68347d3a7734a4a7956c177 |
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| 출처 메모 | uspto-grants-1993_04 |
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