참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Diethyl 2-(5-methyl-3-isoxazolyloxy)malonate | HCID 19986058 | — |
| 반응물 | Aluminium lithium hydride | HCID 21226445 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-O-(5-Methyl-3-isoxazolyl)glycerol | HCID 54330806 | 70.5% |
반응 단계
A solution of 23.72 g of diethyl 2-(5-methyl-3-isoxazolyloxy)malonate (prepared as described in Preparation 19) in 120 ml of tetrahydrofuran was added dropwise to a suspension of 14.00 g of lithium aluminum hydride in 140 ml of tetrahydrofuran over a period of 30 minutes, whilst ice-cooling. The mixture was stirred at room temperature for 40 hours, after which 56 ml of a 4% w/v aqueous solution of sodium hydroxide was added dropwise to it over a period of 30 minutes, whilst ice-cooling. An insoluble material was filtered off using a Celite (trade mark) filter aid, and the filtrate was concentrated by evaporation under reduced pressure. The residue was subjected to column chromatography through 300 g of silica gel. 11.26 g of the title compound was isolated as a colorless oil from the fractions eluted with ethyl acetate.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05068340 |
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| 출처 데이터셋 | uspto-grants-1991_11 |
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| ORD ID | ord-d0633e3606254a05ad8c7ee4d665fd87 |
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| 출처 메모 | uspto-grants-1991_11 |
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