돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 274899생성일: 2026년 10월 25일

Propanoic acid, 3-iodo- → Rhizoxin 3-iodopropionate

https://huagongshe.com/reaction/274899

반응식

참여 물질

역할이름HCID투입량
반응물Propanoic acid, 3-iodo-HCID 8856—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물4-PyrrolidinopyridineHCID 75567—
반응물RhizoxinHCID 6437358—
용매TolueneHCID 1140—
생성물Rhizoxin 3-iodopropionateHCID 8674816780.7%

반응 단계

1.03 g of DCC and a catalytic amount of 4-pyrrolidinopyridine were added to a solution of 1.25 g of rhizoxin and 1.20 g of 3-iodopropionic acid in toluene, and the resulting mixture was stirred at room temperature for 2 hours. At the end of this time, the reaction mixture was treated in the same manner as described in Example 1, to give 1.33 g of rhizoxin 3-iodopropionate. The whole of this ester was immediately dissolved in 20 ml of acetonitrile, and 0.92 g of the silver salt of methylmercaptan prepared at the time of use was added. The resulting mixture was stirred at room temperature for 8 hours, after which the precipitate was filtered off. The solvent was then removed by distillation under reduced pressure, and ethyl acetate was added to the residue. The resulting mixture was washed with a 5% w/v aqueous solution of sodium bicarbonate and with a saturated aqueous solution of sodium chloride, in that order, after which it was dried over anhydrous sodium sulfate. The solvent was then removed by distillation under reduced pressure, and the residue was purified by silica gel column chromatography, using a 1:1 by volume mixture of cyclohexane and ethyl acetate as eluent, to give 970 mg of the title product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05391564
출처 데이터셋uspto-grants-1995_02
ORD IDord-745364b5b29043b39a34a52823d2783a
출처 메모uspto-grants-1995_02