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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 76840생성일: 2026년 10월 25일

5-Amino-2,4,6-triiodo-1,3-benzenedicarboxylic acid → (S)-(-)-5-[(2-Acetoxypropanoyl)amino]-2,4,6-triiodoisophthalic Acid

https://huagongshe.com/reaction/76840

반응식

참여 물질

역할이름HCID투입량
반응물5-Amino-2,4,6-triiodo-1,3-benzenedicarboxylic acidHCID 3015783—
반응물(1S)-2-Chloro-1-methyl-2-oxoethyl acetateHCID 11094804—
용매DimethylacetamideHCID 31374—
생성물(S)-(-)-5-[(2-Acetoxypropanoyl)amino]-2,4,6-triiodoisophthalic AcidHCID 1581730281%

반응 조건

온도50 °C

반응 단계

(S)-1-chloro-1-oxopropan-2-yl acetate (37.4 ml, 295.4 mmol) was added slowly to a suspension of 5-amino-2,4,6-triiodoisophthalic acid (50.0 g, 89.5 mmol) in DMA (100 ml) at a temperature of between 25° C. and 29° C. The resulting mixture was heated to about 50° C. and stirred at this temperature for about 8 hours after which heating was removed and the mixture was stirred for about 14 hours at room temperature. The reaction mixture was added slowly over water (500 ml) with strong stirring at a temperature between 22° C. and 30° C. After addition 300 ml of water were added to the suspension. The suspension was stirred for 5 further hours at about 22° C. after which the white solid was filtered and washed with water previously cooled at about 5° C. twice (30 ml each time). The product was dried in a vacuum oven at about 5.0° C. to yield (S)-5-(2-acetoxypropanamido)-2,4,6-triiodoisophthalic acid (48.8 g, 72.5 mmol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08835672B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-3de18174c3394887ab022402120c5a28
출처 메모uspto-grants-2014_09