참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | 1-Bromoheptane | HCID 12369 | — |
| 반응물 | Heptyltriphenylphosphonium bromide | HCID 2724567 | — |
| 반응물 | Ethyl 5-oxopentanoate | HCID 11137279 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | Hexane | HCID 8058 | — |
| 생성물 | ethyl (Z)-dodec-5-enoate | HCID 5708892 | 99.8% |
반응 단계
Heptyltriphenylphosphonium bromide (16.8g), prepared from 1-bromoheptane and triphenylphosphine analogously to undecyltriphenylphosphonium bromide as described in Example 2(2), is suspended in dry ether (300 ml) and the mixture is treated whilst stirring under nitrogen with 1.7 M butyllithium in hexane (36 ml) from a syringe. The resulting bright red solution is cooled to 10° C. and treated dropwise with ethyl 5-oxopentanoate [5.5 g, prepared as described in Example 2 (1B)] in dry ether (37.5 ml). After 10 minutes, the reaction mixture is worked up by the procedure described in Example 2(2) to give ethyl (Z)-dodec-5-enoate as a yellow oil (8.6g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04844892 |
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| 출처 데이터셋 | uspto-grants-1989_07 |
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| ORD ID | ord-7d3e9c20adec4602852dfb9f2df8d5ea |
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| 출처 메모 | uspto-grants-1989_07 |
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