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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Sodium Hydroxide → HCID 15057240, 화합물

HRID 2073723
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HRID 2073723 반응식
S(Cl)([Cl:3])=O.[Na+].[CH2:6]([S:8]([NH:11][C:12]1[CH:20]=[CH:19][C:15]([C:16]([O-])=[O:17])=[CH:14][CH:13]=1)(=[O:10])=[O:9])[CH3:7].[OH-].[Na+]>O>[CH2:6]([S:8]([NH:11][C:12]1[CH:20]=[CH:19][C:15]([C:16]([Cl:3])=[O:17])=[CH:14][CH:13]=1)(=[O:10])=[O:9])[CH3:7]
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참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 24386Thionyl ChlorideHCID 23706480HCID 23706480, 화합물

생성물 1

HCID 15057240HCID 15057240, 화합물

시약·촉매·용매 1

HCID 962Water용매

실험 절차

To 100 mL of thionyl chloride at 0° C. is added 25.1 g (0.1 mol) of 4-[(ethylsulfonyl)amino]benzoic acid sodium salt (prepared from the acid and sodium hydroxide in water and evaporation of solvent) under a nitrogen atmosphere. Reflux the reaction mixture for 24-40 hr. then remove the excess thionyl chloride in vacuo. Dissolve the crude material in tetrahydrofuran, filter through celite and evaporate the solvent to obtain the title compound.

후처리

  1. temperatureReflux the reaction mixture for 24-40 hr
  2. customthen remove the excess thionyl chloride in vacuo
  3. dissolutionDissolve the crude material in tetrahydrofuran
  4. filtrationfilter through celite
  5. customevaporate the solvent

출처 및 근거

ORD 기록
ord-6ef28d7c3cdc47759ccefda90131641d
출처 데이터셋
uspto-grants-1990_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04920116

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