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5-Bromothiophene-2-sulfonyl chloride → 5-BroMo-thiophene-2-sulfonic acid M ethylaMide

HRID 1351290
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HRID 1351290 반응식
[Br:1][C:2]1[S:6][C:5]([S:7](Cl)(=[O:9])=[O:8])=[CH:4][CH:3]=1.[CH3:11][NH2:12].O1CCCC1>O1CCCC1.O>[CH3:11][NH:12][S:7]([C:5]1[S:6][C:2]([Br:1])=[CH:3][CH:4]=1)(=[O:9])=[O:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 27339245-Bromothiophene-2-sulfonyl chlorideHCID 66615946Methylamine tetrahydrofuran

생성물 1

HCID 15203645-BroMo-thiophene-2-sulfonic acid M ethylaMide

시약·촉매·용매 2

HCID 962Water용매HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 5-bromothiophene-2-sulfonyl chloride (602 mg) in tetrahydrofuran (5 mL) was added dropwise a solution of 2.0M methylamine-tetrahydrofuran (3.5 mL) on an ice bath. After stirring for 15 minutes on an ice bath, the solution was diluted with water and extracted with ethyl acetate. After washing with an aqueous solution of saturated sodium bicarbonate and saturated sodium chloride water, the solution was dried with anhydrous sodium sulfate. After filtration through silica gel, the solvent was removed by evaporation to provide the title compound (608 mg) as a colorless oily matter.

후처리

  1. extractionextracted with ethyl acetate
  2. washAfter washing with an aqueous solution of saturated sodium bicarbonate and saturated sodium chloride water
  3. dry with materialthe solution was dried with anhydrous sodium sulfate
  4. filtrationAfter filtration through silica gel
  5. customthe solvent was removed by evaporation

출처 및 근거

ORD 기록
ord-4099beedcf60446f997ddb36507e5321
출처 데이터셋
uspto-grants-2007_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07217723B2

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