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Iodine chloride → 5-Iodo-4-methyl-2-aminobenzenesulfonamide

HRID 496154
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인쇄 미리보기

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HRID 496154 반응식
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([NH2:11])(=[O:10])=[O:9])=[C:4]([NH2:12])[CH:3]=1.[I:13]Cl>C(Cl)(Cl)Cl>[I:13][C:7]1[C:2]([CH3:1])=[CH:3][C:4]([NH2:12])=[C:5]([S:8]([NH2:11])(=[O:9])=[O:10])[CH:6]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24640Iodine chlorideHCID 114365382-Amino-4-methylbenzenesulfonamide

생성물 1

HCID 223240635-Iodo-4-methyl-2-aminobenzenesulfonamide수율 62.1%

시약·촉매·용매 1

HCID 6212Chloroform용매2회

반응 조건

온도
0 °C

실험 절차

A stirred suspension of 4-methyl-2-aminobenzenesulfonamide (620 mg; 3.3 mmol) in CHCl3 (7 ml) at 0° C. was added a solution of iodine monochloride (1.6 g; 9.9 mmol) in CHCl3 (7 ml). The reaction mixture was stirred at 0° C. until H-NMR indicated full conversion of starting material. The reaction mixture was filtered and the isolated solid washed with small volumes of CHCl3, NaHCO3 (sat. aq.), H2O and air dried to give 640 mg (62%) of product.

후처리

  1. filtrationThe reaction mixture was filtered
  2. washthe isolated solid washed with small volumes of CHCl3, NaHCO3 (sat. aq.), H2O and air
  3. customdried

출처 및 근거

ORD 기록
ord-521c5174335347a4bae92bc57db22b50
출처 데이터셋
uspto-grants-2005_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06943159B1

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