돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2210833생성일: 2026년 10월 25일

12-Bromododecanoic Acid → 12-Chloro-dodecanoic acid

https://huagongshe.com/reaction/2210833

반응식

참여 물질

역할이름HCID투입량
반응물12-Bromododecanoic AcidHCID 175468—
반응물Calcium ChlorideHCID 5284359—
촉매Tetrabutylammonium ChlorideHCID 70681—
용매AcetonitrileHCID 6342—
생성물12-Chloro-dodecanoic acidHCID 381109—

반응 단계

To 12-bromododecanoic acid (1 g) dissolved in acetonitrile (50 ml) was added calcium chloride (2 g) and tetra-n-butylammonium chloride (1.2 g), and the mixture was heated under reflux for 4 hours. The reaction mixture was filtered, concentrated and distributed into ethyl acetate-water, and the ethyl acetate layer was dried over anhydrous sodium sulfate to give 12-chlorododecanoic acid. After a 280 mg portion of 12-chlorododecanoic acid thus obtained, para-nitrophenol (167 mg) and N,N'-dicyclohexylcarbodiimide (245 mg) in N,N-dimethylformamide (DMF) was stirred for 12 hours, precipitates were removed by filtration and DMF was removed by distillation to give an active ester. To the active ester of 12-chlorododecanoic acid dissolved in DMF were added 6-(4'-N-glycyl-spicaminyl-amino)purine hydrochloride (456 mg) and triethylamine (1.2 ml ), and the mixture was stirred for 12 hours. The reaction mixture was concentrated and subjected to chromatography on a silica gel column with eluent systems of chloroform-methanol (from 7:1 to 5:1) to give SPK132 in the yield of mg.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05461036
출처 데이터셋uspto-grants-1995_10
ORD IDord-33ca184a83ca4e71846276d2b3bde25d
출처 메모uspto-grants-1995_10