関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | monoMethyl adipate | HCID 12328 | — |
| 反応物 | Thionyl Chloride | HCID 24386 | — |
| 反応物 | N-bromobutanimide | HCID 67184 | — |
| 生成物 | 2-Bromo-5-carbomethoxypentanoic acid | HCID 14402743 | — |
反応手順
5-Carbomethoxypentanoic acid (12), wherein alk is methyl, was reacted with thionyl chloride and then N-bromosuccinimide (NBS) followed by base hydrolysis to give 2-bromo-5-carbomethoxypentanoic acid (13). Compound (13) was reacted with methyl-3-mercaptopropionate (m=1, R1 '=H and R2 '=OCH3) to yield 5-carbomethoxy-2-[(2-carbomethoxyethyl)thio]-pentanoic acid (14). Compound (14) reacted first with diborane and then with dimethylsulfoxide and trifluoroacetic anhydride to afford 5-carbomethoxy-2-[(2-carbomethoxyethyl)thio]-pentanal (15). Compound (15) was reacted under Wittig conditions with tridecyltriphenylphosphonium ylid to yield methyl-5-[(2-carbomethoxyethyl)thio]-6(Z)-nonadecenoate (16) which was saponified to afford a compound of the formula (IV) wherein m is 1, R1 is hydrogen, and R2 is hydroxyl.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04775662 |
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| 出典データセット | uspto-grants-1988_10 |
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| ORD ID | ord-a8f39c34695d4b838480cf757a46bd6c |
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| 出典メモ | uspto-grants-1988_10 |
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