참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Isopropyltriphenylphosphonium bromide | HCID 2795292 | — |
| 반응물 | 3-Oxo-4,4-dimethyl-5alpha-chola-8,14-dien-24-aldehyde | HCID 15543093 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 반응물 | HCID 178527699 | HCID 178527699 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 4,4-Di methyl-5alpha-cholesta-8,14,24-trien-3-one | HCID 70037746 | 51.7% |
| 생성물 | HCID 178460676 | HCID 178460676 | — |
반응 단계
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%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06645953B2 |
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| 출처 데이터셋 | uspto-grants-2003_11 |
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| ORD ID | ord-06c62459272d4f0c8c49c09c42202482 |
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| 출처 메모 | uspto-grants-2003_11 |
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