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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1606302생성일: 2026년 10월 25일

Pyridine → (Z)-5-Hexadecenal

https://huagongshe.com/reaction/1606302

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Myristoleyl alcoholHCID 5364712—
촉매chromium (VI) trioxideHCID 10219390—
용매DichloromethaneHCID 6344—
생성물(Z)-5-HexadecenalHCID 6430183—

반응 단계

Chromium trioxide (0.56 g. 5.6 mM) is added to a stirred solution of pyridine (0.90 g. 11.4 mM) in methylene chloride (14 ml). The flask is stoppered with a Drieritefilled tube. The deep red solution is stirred for approximately fifteen minutes at room temperature after which a solution of cis-9-tetradecen-1-ol (0.9 mM) in a small amount of methylene chloride (approximately 0.2 ml) is added rapidly and the mixture stirred for another 15 minutes. The product is recovered by decantation from the tarry precipitate, concentrated in vacuo, and the residue extracted with redistilled petroleum ether (Skelly B). This extract is washed successively with dilute aqueous hydrochloric acid (approximately 1%), brine, dilute aqueous sodium bicarbonate (approximately 5%), and brine (until neutral), then filtered through anhydrous magnesium sulfate and evaporated in vacuo to yield 0.17 g. G.c. analysis showed the product contained cis-9-tetradecen-1-ol in approximately 1:9 ratio to the aldehyde, so the product was chromatographed on Florisil (2.4 cm o.d. × 30 cm; packed up to 25 cm) using redistilled benzene (15 ml fractions). Fractions 4 - 7 are combined. Final yield of alcohol-free cis-9-tetradecenal is 60 mg. In accordance with the foregoing procedure but starting with cis-11-hexadecenal in place of cis-9-tetradecenal, there is obtained crude cis-5-hexadecenal (0.19 g.) and alcohol-free cis-11-hexadecenal (0.10 g.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US03952093
출처 데이터셋uspto-grants-1976_04
ORD IDord-f7f505706bfe47e9abae36fa954fa603
출처 메모uspto-grants-1976_04