Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
p-Toluenesulfonic acid → 5-Hexadecene, 16,16-diethoxy-, (5Z)-
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | p-Toluenesulfonic acid | HCID 6101 | — |
| 반응물 | 2-Heptanone | HCID 8051 | — |
| 반응물 | Neral | HCID 643779 | — |
| 반응물 | 11-Hexadecenal, (11Z)- | HCID 5364495 | — |
| 촉매 | Ammonium Chloride | HCID 25517 | — |
| 생성물 | 5-Hexadecene, 16,16-diethoxy-, (5Z)- | HCID 6438017 | 61.5% |
반응 단계
The diethyl acetal or ketal is prepared by the above general procedure from (Z)-11-hexadecenal, (E)-and (Z)-citral in admixture and heptan-2-one using NH4Cl as catalyst in the first two cases and TsOH in the last. (Z)-1,1-Diethoxyhexadec-11-ene is obtained in 61.5% yield and has a b.p. 118°-120° C./0.05 mm, nD20 1.4475; (E)-o and (Z)-1,1-diethoxy-3,7-dimethoxyocta-2,6-diene in admixture are obtained in 83.6% yield and have b.p. 68°-70° C./0.2 mm, nD20 1.4511; 2,2-diethoxyheptane is obtained in 71% yield and has b.p. 88°-92° C./18 mm.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04780479 |
| 출처 데이터셋 | uspto-grants-1988_10 |
| ORD ID | ord-86414a1034c44b1eb37d5bf52d00e73a |
| 출처 메모 | uspto-grants-1988_10 |