참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tetrakis(hydroxymethyl)phosphonium chloride | HCID 31298 | — |
| 반응물 | 4-(2,2-Dimethoxyethyl)hepta-1,6-dien-4-ol | HCID 86614113 | — |
| 촉매 | HCID 178425456 | HCID 178425456 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Isopropanol | HCID 3776 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Sodium Hydroxide | HCID 14798 | — |
| 생성물 | 2,2-Dimethoxyethylcyclopent-3-enol | HCID 67306500 | — |
반응 단계
A solution of 4-(2,2-dimethoxyethyl)hepta-1,6-dien-4-ol (28 g, 140 mmol) in DCM (2 L) was charged to a 3 L RB flask. Dry argon was bubbled through the solution for ˜30 minutes. Grubbs second generation catalyst (5.9 g, 7.0 mmol) was added and the reaction was allowed to stir under argon for 15 hours. The reaction was quenched with a solution of tetrakis-(hydroxymethyl)phosphonium chloride (27 g, 140 mmol) in isopropanol (200 mL) and 10 N NaOH (14 mL), and stirred for 15 hours. The reaction was diluted with water (1 L) and poured into a seperatory funnel. The DCM layer was separated and the aqueous was extracted with DCM (3×100 mL). The combined organics were concentrated to a dark oil which was purified by flash chromatography on a 330 g ISCO column eluting by gradient hexanes to 20% EtOAc/hexanes over a 50 minute period. Product fractions were combined to afford the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07973047B2 |
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| 출처 데이터셋 | uspto-grants-2011_07 |
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| ORD ID | ord-2d83a5ed07d74287b7298e1263f209aa |
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| 출처 메모 | uspto-grants-2011_07 |
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