Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3989생성일: 2026년 10월 23일
2,3-Dihydroxybutanedioic Acid → 2-[3-[(Phenylethyl)methylamino]-propyl]-2-isopropylphenylacetaldehyde
https://huagongshe.com/ko/reaction/3989
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2,3-Dihydroxybutanedioic Acid | HCID 875 | — |
| 반응물 | Sulfuric Acid | HCID 1118 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | 5-[Methyl(2-phenylethyl)amino]-2-phenyl-2-propan-2-ylpentanenitrile | HCID 71225 | — |
| 반응물 | Diisobutylaluminumhydride | HCID 21225700 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | Hexane | HCID 8058 | — |
| 생성물 | 2-[3-[(Phenylethyl)methylamino]-propyl]-2-isopropylphenylacetaldehyde | HCID 88638019 | — |
반응 단계
180 ml of a 1M solution of diisobutylaluminum hydride in hexane were added dropwise, at -5° C., to a solution of 33.4 g (0.1 mole) of 2-[3-[(phenylethyl)-methylamino]-propyl]-isopropylphenylacetonitrile in 400 ml of diethyl ether. The mixture was stirred for 1.5 hours, after which 500 ml of 10% strength sulfuric acid were added. 30 g of tartaric acid were introduced, the mixture was rendered alkaline with concentrated potassium hydroxide solution, and the ether phase was separated off and washed several times with sodium chloride solution. After the ether phase had been dried over sodium sulfate, the ether was distilled off, the remaining oily residue was dissolved in 300 ml of ethyl acetate, and hydrochloric acid in isopropanol was added. The mixture was left to stand overnight, after which the precipitated hydrochloride was filtered off under suction.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04723039 |
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| 출처 데이터셋 | uspto-grants-1988_02 |
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| ORD ID | ord-9e27edb996dc4b2e8698c669aeab451a |
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| 출처 메모 | uspto-grants-1988_02 |
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