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HRID 231004생성일: 2026년 10월 25일

Triphenylphosphine → ethyl (Z)-dodec-5-enoate

https://huagongshe.com/reaction/231004

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참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물1-BromoheptaneHCID 12369—
반응물Heptyltriphenylphosphonium bromideHCID 2724567—
반응물Ethyl 5-oxopentanoateHCID 11137279—
반응물ButyllithiumHCID 178418339—
용매Diethyl EtherHCID 3283—
용매HexaneHCID 8058—
생성물ethyl (Z)-dodec-5-enoateHCID 570889299.8%

반응 조건

온도10 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04844892
출처 데이터셋uspto-grants-1989_07
ORD IDord-7d3e9c20adec4602852dfb9f2df8d5ea
출처 메모uspto-grants-1989_07