참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Allyl chloride | HCID 7850 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | 3-Methyl-2-(2-methylphenyl)butanenitrile | HCID 14245130 | — |
| 촉매 | Tetrabutylammonium hydrogen sulfate | HCID 94433 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | alpha-Allyl-alpha-isopropyl-2-methylbenzyl cyanide | HCID 19933531 | 93% |
반응 단계
To a solution of 362 g of sodium hydroxide in 362 ml of demineralized water 216.6 g of α-isopropyl-2-methylbenzyl cyanide and 6.4 g of tetrabutylammonium hydrogen sulfate were added, and the mixture was heated to 40° C. with intensive stirring. During 3hours 287 g of allylchloride was added. During, the addition and for further two hours the temperature of the reaction mixture was maintained at 40° C. and thereafter at 60° C. for additional three hours. After cooling to room temperature, the reaction mixture was diluted with 550 ml of water and the product was extracted into toluene. After washing with water until neutral pH and drying with anhydrous magnesium sulfate, the solvent was evaporated and the residue was distilled under diminished pressure to obtain 249 g (93%) of the desired compound, b.p. 122°-124 ° C./333 Pa.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05424456 |
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| 출처 데이터셋 | uspto-grants-1995_06 |
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| ORD ID | ord-4885e1af76354a0da3de3354ae290034 |
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| 출처 메모 | uspto-grants-1995_06 |
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