Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1249229생성일: 2026년 10월 26일
Tetrahydrofuran → 4-(4-Morpholino-3-nitrophenyl)-4-(cyano)-4-(morpholino)-3-methylbutyronitrile
https://huagongshe.com/reaction/1249229
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | Crotononitrile | HCID 637921 | — |
| 반응물 | alpha-Morpholino-alpha(4-morpholino-3-nitrophenyl)-acetonitrile | HCID 21855724 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 4-(4-Morpholino-3-nitrophenyl)-4-(cyano)-4-(morpholino)-3-methylbutyronitrile | HCID 20164991 | — |
반응 단계
A solution of 8.0 parts of crotononitrile in 20 parts by volume of tetrahydrofuran is added to a stirred mixture of 16.5 parts of α-morpholino-α(4-morpholino-3-nitrophenyl)-acetonitrile in 150 parts by volume of tetrahydrofuran and 1.5 parts of potassium hydroxide in 5 parts by volume of methanol at room temperature under an atmosphere of nitrogen. The reaction mixture is stirred for a further 6 hours, diluted with 500 parts by volume of water and extracted with 4×250 parts by volume of ethyl acetate. The combined organic extracts are dried over magnesium sulphate and concentrated under vacuum. The resulting crude product is triturated with a mixture of 50 parts by volume of ethyl acetate and hexane. The solid product is collected, washed with ethyl acetate and dried at 80° under vacuum to give 4-(4-morpholino-3-nitrophenyl)-4-(cyano)-4-(morpholino)-3-methylbutyronitrile having melting point 175°-177° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04629789 |
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| 출처 데이터셋 | uspto-grants-1986_12 |
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| ORD ID | ord-833f64a256f84e5880a1459d0da9a247 |
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| 출처 메모 | uspto-grants-1986_12 |
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