참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Water | HCID 962 | — |
| 반응물 | 5-(Benzyloxy)-2-nitrobenzaldehyde | HCID 3849835 | — |
| 반응물 | HCID 178456138 | HCID 178456138 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-[5-(Benzyloxy)-2-nitrophenyl]-2-methyl-2-propen-1-ol | HCID 23003065 | 48.7% |
반응 단계
35.9 ml (16.33 mmol) of a 0.5 M isopropenylmagnesium bromide solution in THF are slowly added at −78° C. to a solution of 3.0 g (11.66 mmol) of 5-benzyloxy-2-nitrobenzaldehyde in 50 ml of THF. After addition is complete, the mixture is stirred at −78° C. for 2 h, then treated with 40 ml of water and warmed to room temperature. The mixture is treated with 10 ml of 1 N hydrochloric acid, the aqueous phase is extracted 2× with ethyl acetate, and the combined organic extracts are dried over sodium sulphate and freed from the solvent in vacuo. Purification of the crude product on silica gel (CH2Cl2) affords 1.7 g (48.7%) of 1-[5-(benzyloxy)-2-nitrophenyl]-2-methyl-2-propen-1-ol as a yellow oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06608049B2 |
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| 출처 데이터셋 | uspto-grants-2003_08 |
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| ORD ID | ord-eb354f2a15d44414b896dc3d2e9aa075 |
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| 출처 메모 | uspto-grants-2003_08 |
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