참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3-Bromo-2-methyl-1-propene | HCID 357785 | — |
| 반응물 | Methyl [3,5-bis(benzyloxy)phenyl]acetate | HCID 640121 | — |
| 반응물 | Lithium diisopropylamide | HCID 2724682 | — |
| 반응물 | Tetrahydrofuran heptane ethylbenzol | HCID 22742125 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-(3,5-Bis-benzyloxyphenyl)-4-methyl-pent-4-enoic acid methyl ester | HCID 57755039 | 94.3% |
반응 단계
A 2M solution of LDA in THF-heptane-ethylbenzene (21.5 mL, 43.0 mmol) was added dropwise over 12 min to a stirred solution of (3,5-bis-benzyloxyphenyl)acetic acid methyl ester (13.0 g, 35.9 mmol) in THF (80 mL) at −78° C. under a nitrogen atmosphere. The temperature was maintained below −70° C. for a further 50 min then 3-bromo-2-methylpropene (4.0 mL, 39.7 mmol) was added in one portion and the reaction mixture was warmed to 0° C. After 2 h the mixture was concentrated in vacuo, diluted with sat. aq. NH4Cl (100 mL) and extracted with EtOAc (100 mL). The organic layer was washed with brine (100 mL), dried (MgSO4), concentrated in vacuo and purified by flash chromatography (silica, 0-10% EtOAc in petroleum ether) to afford the title product as a yellow oil (14.1 g, 94%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07557244B2 |
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| 출처 데이터셋 | uspto-grants-2009_07 |
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| ORD ID | ord-e4cd3a373ea64c1397c60db3820a9fa0 |
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| 출처 메모 | uspto-grants-2009_07 |
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