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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 879035생성일: 2026년 10월 25일

Dimethyl Sulfoxide → 11-Hexadecenal, (11Z)-

https://huagongshe.com/reaction/879035

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물TriethylamineHCID 8471—
반응물Oxalyl chlorideHCID 65578—
반응물VirelureHCID 5283305—
용매Diethyl EtherHCID 3283—
용매DichloromethaneHCID 6344—
생성물11-Hexadecenal, (11Z)-HCID 536449595%

반응 단계

DMSO (0.11 mL, 1.6 mmol) was added dropwise to a solution of oxalyl chloride (0.080 mL, 0.96 mmol) in CH2Cl2 (5 mL) at −78° C., and after 5 minutes a solution of alcohol 5 (0.21 g, 0.87 mmol) in CH2Cl2 (0.9 mL) was added. After stirring for 15 minutes at the same temperature, triethylamine (0.61 mL, 4.4 mmol) was added. The mixture was warmed to room temperature, diluted with Et2O, washed sequentially with 1M HCl, saturated aqueous NaHCO3, brine, dried with Na2SO4, and the solvent was removed in vacuo. Flash chromatography of the residue (SiO2, 10% EtOAc in hexanes) provided 6 (0.20 g, 95% yield, 86% Z as determined by 1H-NMR) as a colorless oil; 1H NMR (CDCl3): δ 9.76 (1H, t, J=1.9 Hz), 5.36 (2H, m), 2.42 (2H, td, J=7.4, 1.9 Hz), 2.02 (4H, m), 1.63 (2H, m), 1.24-1.36 (16H, m), 0.90 (3H, t, J=7.2 Hz); 13C NMR (CDCl3): δ 202.9, 129.9, 129.8, 43.9, 32.0, 29.8, 29.5, 29.4 (2C), 29.3, 29.2, 27.2, 26.9, 22.4, 22.1, 14.0; HRMS (FAB): 237.2209, [C16H30O−H]+ requires 237.2218.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08987531B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-8a33d951905d466c8104057395d84a13
출처 메모uspto-grants-2015_03