참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | 3-Methoxy-4-(methoxymethoxy)benzaldehyde | HCID 79661 | — |
| 반응물 | Phosphonium, (3-hydroxypropyl)triphenyl-, bromide | HCID 11025793 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (E)-4-[3-Methoxy-4-(methoxymethoxy)phenyl]-3-buten-1-ol | HCID 20071447 | 35.5% |
반응 단계
n-Butyllithium (1.6 M in hexane, 25 ml) was added dropwise to a stirred suspension of (3-hydroxypropyl)triphenylphosphonium bromide (8.03 g) in dry THF (50 ml) cooled to 0° under nitrogen. The resulting blood-red solution was stirred at 0° for 10 min and then 3methoxy-4-(methoxymethoxy)benzaldehyde (3.60 g) in dry THF (10 ml) was added dropwise over 5 min. The mixture was allowed to warm to room temperature, stirred for 4 h water (10 ml) was added and the majority of the solvent was removed in vacuo at 40°. A solution of the residual oil in ER (200 ml) was washed with water (150 ml), dried, treated with charcoal, concentrated and purified by [FCS] eluting with EA/hexane (1:1) to give the title compound (1.55 g). T.l.c. (EA-hexane 1:1) Rf 0.30.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04990505 |
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| 출처 데이터셋 | uspto-grants-1991_02 |
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| ORD ID | ord-4aa5abc2b64446508fa58debd6b181ef |
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| 출처 메모 | uspto-grants-1991_02 |
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