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Hydrochloric Acid → 4-Formyl-N-[4-(trifluoromethoxy)phenyl]benzene-1-sulfonamide

HRID 1696615
ノート
印刷プレビュー

反応式

HRID 1696615 の反応式
Cl[S:2]([C:5]1[CH:12]=[CH:11][C:8]([CH:9]=[O:10])=[CH:7][CH:6]=1)(=[O:4])=[O:3].[F:13][C:14]([F:24])([F:23])[O:15][C:16]1[CH:22]=[CH:21][C:19]([NH2:20])=[CH:18][CH:17]=1.N1C=CC=CC=1.Cl>ClC(Cl)C>[CH:9]([C:8]1[CH:11]=[CH:12][C:5]([S:2]([NH:20][C:19]2[CH:21]=[CH:22][C:16]([O:15][C:14]([F:13])([F:23])[F:24])=[CH:17][CH:18]=2)(=[O:4])=[O:3])=[CH:6][CH:7]=1)=[O:10]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 1049PyridineHCID 6008484-(Trifluoromethoxy)anilineHCID 27592104-Formylbenzene-1-sulfonyl chloride

生成物 1

HCID 714239844-Formyl-N-[4-(trifluoromethoxy)phenyl]benzene-1-sulfonamide収率 46.3%

試薬・触媒・溶媒 1

HCID 6365
1,1-Dichloroethane
溶媒

実験手順

to a mixture of 610 mg of 4-chlorosulfonylbenzaldehyde (3 mmoles) and 460 mg of 4-trifluoromethoxyaniline (3 mmoles) in 2 ml of dichloroethane is added 2 ml of pyridine (25 mmoles). The reaction mixture is stirred at room temperature for 5 hours and then poured into 100 ml of 10% HCl solution. The mixture is extracted twice with 30 ml of DCM. The combined organic extracts are washed with 30 ml of water, 30 ml of a saturated solution of sodium bicarbonate and brine, and the solution is dried over MgSO4 and concentrated. The crude product is purified on silica gel using DCM/AcOEt 90/10 as eluent. 0.48 g of 4-formyl-N-(4-trifluoromethoxy-phenyl)-benzenesulfonamide is isolated as a white solid (yield=47%). Analytical LC/MS method A:([M+H]+): 346, RT: 5.53 min (gradient 5 to 85% acetonitrile in 7 min).

後処理

  1. extractionThe mixture is extracted twice with 30 ml of DCM
  2. washThe combined organic extracts are washed with 30 ml of water, 30 ml of a saturated solution of sodium bicarbonate and brine
  3. dry with materialthe solution is dried over MgSO4
  4. concentrationconcentrated
  5. customThe crude product is purified on silica gel

出典と根拠

ORDレコード
ord-5487a8715ad746b0992cb861cd8ae5fc
出典データセット
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08163768B2

反応ノート

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