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Carbon tetrabromide → 4-Bromomethylbenzenesulfonamide

HRID 1162193
ノート
印刷プレビュー

反応式

HRID 1162193 の反応式
O[CH2:2][C:3]1[CH:8]=[CH:7][C:6]([S:9]([NH2:12])(=[O:11])=[O:10])=[CH:5][CH:4]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C(Br)(Br)(Br)[Br:33]>C(Cl)Cl>[Br:33][CH2:2][C:3]1[CH:8]=[CH:7][C:6]([S:9]([NH2:12])(=[O:11])=[O:10])=[CH:5][CH:4]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 11205Carbon tetrabromideHCID 11776TriphenylphosphineHCID 100811624-(Hydroxymethyl)benzenesulfonamide

生成物 1

HCID 131545004-Bromomethylbenzenesulfonamide収率 50%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

4-hydroxymethyl-benzene-sulphonamide (0.105 mg, 0.56 mmoles) was dissolved in DCM (5 mL). Polymer supported triphenylphosphine (294 mg, 2.4 mmoles/g, 1.12 mmoles) was added, and the mixture was stirred with a shaker at room temperature for 10 minutes. CBr4 (557 mg, 1.68 mmoles) was then added, and stirring was continued for 3 hours. The supported reagent was removed by filtration, the solvent was evaporated, and the crude material was purified by flash chromatography (SiO2, petroleum ether/AcOEt 9/1) to yield the title compound as a light-yellow solid (70 mg).

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. additionwas added
  2. stirringstirring
  3. waitwas continued for 3 hours
  4. customThe supported reagent was removed by filtration
  5. customthe solvent was evaporated
  6. customthe crude material was purified by flash chromatography (SiO2, petroleum ether/AcOEt 9/1)

出典と根拠

ORDレコード
ord-959b2cf596024fef80905e822d391f51
出典データセット
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07820698B2

反応ノート

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