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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Methylamine → 2-Hydroxyphenyl methylsulfamate

HRID 1022728
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HRID 1022728 반응식
[O:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[O:3][S:2]1(=[O:11])=[O:10].[CH3:12][NH2:13]>C1COCC1.C(OCC)(=O)C>[CH3:12][NH:13][S:2](=[O:11])(=[O:10])[O:1][C:5]1[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=1[OH:3]
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참가 물질

5

반응물 2

HCID 6329MethylamineHCID 37776671,3,2Lambda6-benzodioxathiole-2,2-dione

생성물 1

HCID 669759552-Hydroxyphenyl methylsulfamate

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매HCID 8857Ethyl Acetate용매

실험 절차

To a solution of 1,3,2-benzodioxathiol 2,2-dioxide (300 mg) in THF (6 mL) was added methylamine (0.871 mL, 2 M THF solution) at room temperature, and the mixture was stirred at room temperature for 3 hr. The reaction mixture was diluted with ethyl acetate. The diluted solution was washed with distilled water and brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel chromatography (hexane/ethyl acetate) to give the title compound (86 mg).

후처리

  1. washThe diluted solution was washed with distilled water and brine
  2. dry with materialdried over anhydrous magnesium sulfate
  3. customThe solvent was evaporated under reduced pressure
  4. customthe residue was purified by silica gel chromatography (hexane/ethyl acetate)

출처 및 근거

ORD 기록
ord-fec88b87266840f0870fc48372b7a6b2
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08722662B2

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