関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Tetrahydropyranyl ether | HCID 263182 | — |
| 反応物 | 6-Ketoprostaglandin F1 alpha | HCID 5280888 | — |
| 反応物 | Jones' reagent | HCID 131709961 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 生成物 | Tetrahydropyranyl ether | HCID 263182 | — |
| 生成物 | 6-Keto-PGE1 | HCID 5280889 | — |
反応手順
The reaction product from part A, containing 6-keto-PGF1α, bis(tetrahydropyranyl)ether, methyl ester corresponding to formula IV, is oxidized to compound V. A composite from several lots, weighing 0.93 g., in 20 ml. of acetone is treated at -10° C. with 2.0 ml. of Jones reagent. After stirring for 1.5 hr. the reaction mixture is quenched with isopropanol and extracted with diethyl ether. The extract is washed with brine, dried, and concentrated. The residue is subjected to silica gel chromatography, eluting with ethyl acetate (20-50%)-Skellysolve B to yield the formula-V 6-keto-PGE1, bis(tetrahydropyranyl)ether, methyl ester, 0.52 g., having Rf 0.52 (TLC on silica gel in ethyl acetate-Skellysolve B (1:1)); and infrared peaks at 1745 and 1725 cm-1 (free of OH at 3000-3500).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04124601 |
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| 出典データセット | uspto-grants-1978_11 |
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| ORD ID | ord-ddb5f52ad53f43148906cd287b3f63a4 |
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| 出典メモ | uspto-grants-1978_11 |
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