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Water → 2-Aminoresorcinol ditosylate

HRID 337342
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HRID 337342 반응식
[NH2:1][C:2]1[C:7]([OH:8])=[CH:6][CH:5]=[CH:4][C:3]=1[OH:9].C(N([CH2:15][CH3:16])CC)C.[C:17]1([CH3:27])[CH:22]=[CH:21][C:20]([S:23](Cl)(=[O:25])=[O:24])=[CH:19][CH:18]=1.[OH2:28]>ClCCl>[CH3:27][C:17]1[CH:22]=[CH:21][C:20]([S:23]([O:9][C:3]2[CH:4]=[CH:5][CH:6]=[C:7]([O:8][S:23]([C:20]3[CH:21]=[CH:22][C:15]([CH3:16])=[CH:18][CH:19]=3)(=[O:24])=[O:28])[C:2]=2[NH2:1])(=[O:25])=[O:24])=[CH:19][CH:18]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 73974-Toluenesulfonyl chlorideHCID 8471TriethylamineHCID 694512-Aminoresorcinol

생성물 1

HCID 867032532-Aminoresorcinol ditosylate

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

100 mg of 2-aminobenzene-1,3-diol was dissolved in 2 ml of dichloromethane, and 234 μl of triethyl amine and 320 mg of p-toluene sulfonyl chloride were added and stirred at room temperature for 1.5 hours. To the reaction mixture, 20 ml of water was added, and extracted with 20 ml of ethyl acetate. After the organic layer was dried over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure, and purified by silica gel column chromatography (hexane:ethyl acetate=4:1) to yield 278.1 mg of the title compound.

후처리

  1. extractionextracted with 20 ml of ethyl acetate
  2. dry with materialAfter the organic layer was dried over anhydrous magnesium sulfate
  3. distillationthe solvent was distilled off under reduced pressure
  4. custompurified by silica gel column chromatography (hexane:ethyl acetate=4:1)

출처 및 근거

ORD 기록
ord-2d8aa5891f7b4dbcbda57d5c695a9ac8
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08889727B2

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