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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2106627생성일: 2026년 10월 26일

1-Bromododecane → 2,2'-[2-Dodecylthio-1,3,5-triazine-4,6-diylbis-(thio)]bis dodecanoic acid

https://huagongshe.com/reaction/2106627

반응식

참여 물질

역할이름HCID투입량
반응물1-BromododecaneHCID 8919—
반응물Potassium HydroxideHCID 14797—
반응물2-Bromododecanoic acidHCID 66980—
반응물Trithiocyanuric AcidHCID 1268121—
용매EthanolHCID 702—
생성물2,2'-[2-Dodecylthio-1,3,5-triazine-4,6-diylbis-(thio)]bis dodecanoic acidHCID 5417282879.2%

반응 단계

A stirred solution of KOH (5.6 g; 0.1 mole) in ethanol (100 ml) is cooled to 5-10° C. and treated with trithiocyanuric acid (4.42 g; 0.025 mole). After stirring for 30 minutes, the reaction mixture is treated with 2-bromododecanoic acid (13.9 g; 0.05 mole) in small portions over 10-15 minutes. The resulting white suspension is stirred for a further 30 minutes at 10° C. and is then allowed to warm to ambient temperature. Upon reaching ambient temperature, the reaction mixture is heated to reflux and maintained at this temperature for 3 hours. The reaction mixture is then cooled to 5° C. and treated with a solution of KOH (1.4 g; 0.025 mole) in ethanol (50 ml) followed by dodecyl bromide (6.2 g; 0.025 mole). The reaction mixture is allowed to warm to ambient temperature and is then heated to reflux and maintained at this temperature for 2 hours. The reaction mixture is cooled to ambient temperature and the solvent removed under reduced pressure. The residue is suspended in water (100 ml and acidified with concentrated HCl to pH 3. The acidified aqueous suspension is then extracted with either (200 ml) and the ether extract is washed with water (3×50 ml). The extract is dried over MgSO4, filtered, then evaporated to yield 14.7 g (79 %) of a yellow viscous oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04931196
출처 데이터셋uspto-grants-1990_06
ORD IDord-043277330df84e5c906f026bc99bbdc0
출처 메모uspto-grants-1990_06