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Pyridine → 1,3,5-Triiodobenzene-2,4,6-trialdehyde

HRID 383000
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HRID 383000 반응식
[I:1][C:2]1[C:7]([CH2:8][OH:9])=[C:6]([I:10])[C:5]([CH2:11][OH:12])=[C:4]([I:13])[C:3]=1[CH2:14][OH:15].C(N(CC)CC)C.N1C=CC=CC=1>CS(C)=O>[I:1][C:2]1[C:3]([CH:14]=[O:15])=[C:4]([I:13])[C:5]([CH:11]=[O:12])=[C:6]([I:10])[C:7]=1[CH:8]=[O:9]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1049PyridineHCID 8471TriethylamineHCID 206936271,3,5-Triiodo-2,4,6-trihydroxymethylbenzene

생성물 1

HCID 184293191,3,5-Triiodobenzene-2,4,6-trialdehyde

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

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온도
0 °C

실험 절차

1,3,5-Triiodo-2,4,6-trihydroxymethylbenzene (4.5 g, 8.2 mmol) was dissolved in DMSO (80 ml). Triethylamine (51.7 ml, 371 mmol) and pyridine. SO3 (11.8 g, 74.2 mmol) were added and the mixture was stirred for two hours. The two phases were separated and the lower phase was cooled to 0° C., poured into water (150 ml) and stirred for 30 min at 0° C. The white solid was collected by filtration, washed with water and dried. Yield: 3.0 g (67%).

후처리

  1. additionSO3 (11.8 g, 74.2 mmol) were added
  2. customThe two phases were separated
  3. additionpoured into water (150 ml)
  4. stirringstirred for 30 min at 0° C
  5. filtrationThe white solid was collected by filtration
  6. washwashed with water
  7. customdried

출처 및 근거

ORD 기록
ord-f3dcd7a752cf42448ded2472fe4cb84b
출처 데이터셋
uspto-grants-2001_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06310243B1

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