関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Magnesium | HCID 5462224 | — |
| 反応物 | (Z)-1-Bromo-4-decene | HCID 10932932 | — |
| 反応物 | (Z)-2-((Z)-Dec-4-en-1-yl)dodec-6-enal | HCID 89768339 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (6Z,16Z)-12-((Z)-dec-4-enyl)docosa-6,16-dien-11-ol | HCID 89775018 | 76% |
反応手順
To a suspension of magnesium turnings (0.6 g, 23.9 mmol) in tetrahydrofuran (5 mL) was slowly added a solution of (Z)-1-bromodec-4-ene 3 (4.5 g, 20.5 mmol) in tetrahydrofuran (5 mL). The reaction mixture was stirred for 30 minutes at room temperature then a solution of (Z)-2-((Z)-dec-4-enyl)dodec-6-enal 7 in tetrahydrofuran (5 mL) was added. The solution was stirred for 15 minutes at room temperature then poured into 5% hydrochloric acid (50 mL) and ice (100 mL). The solution was extracted with ether (2×150 mL). The combine ether extracts were dried on magnesium sulfate, filtered, and concentrated in vacuo to dryness. The residue was purified by column chromatography (1% ethyl acetate in hexanes) to afford (6Z,16Z)-12-((Z)-dec-4-enyl)docosa-6,16-dien-11-ol 8 as a colorless oil (4.8 g, 76%). Rf 0.45 (10% EtOAc-Hexanes).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09352042B2 |
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| 出典データセット | uspto-grants-2016_05 |
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| ORD ID | ord-5fb82f821f6f41ffa5b365403468eadd |
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| 出典メモ | uspto-grants-2016_05 |
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