참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Diiodomethane | HCID 6346 | — |
| 반응물 | Lithium diisopropylamide | HCID 2724682 | — |
| 반응물 | 2H-Pyran-4-carboxylic acid, tetrahydro-, methyl ester | HCID 2773520 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 4-Iodomethyl-tetrahydro-pyran-4-carboxylic acid methyl ester | HCID 22719788 | 53% |
반응 단계
Lithium diisopropylamide (10.9 ml of 2.0M solution in heptane/tetrahydrofuran/ethylbenzene) was added to a stirred solution of tetrahydropyran-4-carboxylic acid methyl ester (3.00 g) in tetrahydrofuran (50 ml) at 0° C. under an atmosphere of nitrogen. The mixture was stirred for 30 minutes before dropwise addition of diiodomethane (2.51 ml). Stirring was continued for a further hour during which it warmed to room temperature. The reaction was poured into water (50 ml) and then extracted with diethyl ether (3×40 ml). The combined organics were washed with water (2×20 ml), 2 M hydrochloric acid (20 ml), water (20 ml) and brine (20 ml). After drying (MgSO4), filtering and evaporating under reduced pressure a yellow oil was obtained which was purified by column chromatography eluting with 3.1 hexane/diethyl ether to give the title compound as a colourless oil (3.11 g, 53%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06809100B2 |
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| 출처 데이터셋 | uspto-grants-2004_10 |
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| ORD ID | ord-cf4f3324b8dd4eedbca6d88137116b8c |
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| 출처 메모 | uspto-grants-2004_10 |
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