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2-Amino-3,5-dibromobenzene-1-sulfonyl fluoride → 2,4-Dibromo-6-(methylsulfonyl)aniline

HRID 1995456
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HRID 1995456 반응식
F[S:2]([C:5]1[CH:11]=[C:10]([Br:12])[CH:9]=[C:8]([Br:13])[C:6]=1[NH2:7])(=[O:4])=[O:3].[CH3:14][Li]>CCOCC>[Br:13][C:8]1[CH:9]=[C:10]([Br:12])[CH:11]=[C:5]([S:2]([CH3:14])(=[O:4])=[O:3])[C:6]=1[NH2:7]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 132189042-Amino-3,5-dibromobenzene-1-sulfonyl fluorideHCID 178418348HCID 178418348, 화합물

생성물 1

HCID 132189052,4-Dibromo-6-(methylsulfonyl)aniline

시약·촉매·용매 1

HCID 3283Diethyl Ether용매2회

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온도
0 °C

실험 절차

A solution of 2-fluorosulfonyl-4,6-dibromoaniline (7.19 g; 0.0216 mol) in ether (100 ml) is cooled to -65° C. under a nitrogen atmosphere and a solution of methyllithium in ether (37.5 ml of 1.8 M; 0.0675 mol) is added via a syringe. The mixture is allowed to warm to 0° C., the solution is poured into ice, and the ether layer is separated. The aqueous layer is extracted with ether (3×100 ml) and the ether layers are combined. The solvent is removed under reduced pressure and the residue crystallized from petroleum ether to afford the title product.

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후처리

  1. additionthe solution is poured into ice
  2. customthe ether layer is separated
  3. extractionThe aqueous layer is extracted with ether (3×100 ml)
  4. customThe solvent is removed under reduced pressure
  5. customthe residue crystallized from petroleum ether

출처 및 근거

ORD 기록
ord-74c4c2aef08e4151943501baf933121d
출처 데이터셋
uspto-grants-1983_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04404402

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