참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | 4-Chloro-alpha,alpha,alpha-trifluoro-3-nitrotoluene | HCID 8462 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | Benzyldodecyldimethyl ammonium chloride | HCID 53445721 | — |
| 용매 | 2-Methoxyethanol | HCID 8019 | — |
| 생성물 | 2-Nitro-4-(trifluoromethyl)phenol | HCID 9816 | 92% |
반응 단계
45 g of 4-chloro-3-nitro-benzotrifluoride and 10 ml of 50% strength aqueous benzyldodecyldimethylammonium chloride are initially introduced into 150 ml of ethylene glycol monomethyl ether, and 100 g of 50% strength potassium hydroxide solution are added dropwise in the course of about 30 minutes, up to a temperature of 65° C. The mixture is then stirred at 65° C. for 6 hours and subsequently cooled and rendered acid with concentrated hydrochloric acid, and about 500 ml of distillate are driven over with steam. The organic phase is separated off and washed with 20 ml of dilute hydrochloric acid, and the organic phase is again separated off and dried with sodium sulphate. 38 g of 2-nitro-4-trifluoromethylphenol are obtained, which corresponds to a yield of 92% of theory.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04225731 |
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| 출처 데이터셋 | uspto-grants-1980_09 |
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| ORD ID | ord-dd14553770ba48f4a69e66321c63b24e |
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| 출처 메모 | uspto-grants-1980_09 |
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