関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | 3-Methoxy-4-(methoxymethoxy)benzaldehyde | HCID 79661 | — |
| 反応物 | Phosphonium, (3-hydroxypropyl)triphenyl-, bromide | HCID 11025793 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (E)-4-[3-Methoxy-4-(methoxymethoxy)phenyl]-3-buten-1-ol | HCID 20071447 | 35.5% |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04990505 |
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| 出典データセット | uspto-grants-1991_02 |
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| ORD ID | ord-4aa5abc2b64446508fa58debd6b181ef |
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| 出典メモ | uspto-grants-1991_02 |
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