関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | Isopropyltriphenylphosphonium bromide | HCID 2795292 | — |
| 反応物 | 3-Oxo-4,4-dimethyl-5alpha-chola-8,14-dien-24-aldehyde | HCID 15543093 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 反応物 | HCID 178527699 | HCID 178527699 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 4,4-Di methyl-5alpha-cholesta-8,14,24-trien-3-one | HCID 70037746 | 51.7% |
| 生成物 | HCID 178460676 | HCID 178460676 | — |
反応手順
A solution of isopropyltriphenylphosphorane was prepared by addition of BuLi (0.16 ml of 1.6M in hexanes, 0.26 mmol) to a suspension of isopropyltriphenylphosphonium bromide (98 mg, 0.26 mmol) in THF (2 mL) at ice bath temperature. The corresponding deep red phosphorane solution was stirred a further 0.5 hour and then added dropwise via syringe to a solution of 3-oxo-4,4-dimethyl-5α-chola-8,14-dien-24-aldehyde (71 mg, 0.18 mmol) in THF (2ml) at −78° C. and stirred 2 hours before slowly warming to room temperature and stirring overnight. Saturated ammonium chloride (3 mL) was added and the aqueous phase extracted using diethyl ether, and the organic phase dried over anhydrous sodium sulphate. Flash chromatography (Eluant: 6 hexane: 1 ethyl acetate) gave the title compound (38 mg, 50%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06645953B2 |
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| 出典データセット | uspto-grants-2003_11 |
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| ORD ID | ord-06c62459272d4f0c8c49c09c42202482 |
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| 出典メモ | uspto-grants-2003_11 |
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