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Bromine → 3'-(2-Bromoacetyl)-4'-fluoromethanesulfonanilide

HRID 2379183
ノート
印刷プレビュー

反応式

HRID 2379183 の反応式
[C:1]([C:4]1[CH:5]=[C:6]([CH:12]=[CH:13][C:14]=1[F:15])[NH:7][S:8]([CH3:11])(=[O:10])=[O:9])(=[O:3])[CH3:2].[Br:16]Br>C(O)(=O)C>[Br:16][CH2:2][C:1]([C:4]1[CH:5]=[C:6]([CH:12]=[CH:13][C:14]=1[F:15])[NH:7][S:8]([CH3:11])(=[O:10])=[O:9])=[O:3]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 24408BromineHCID 111071753'-Acetyl-4'-fluoromethanesulfonanilide

生成物 1

HCID 221413933'-(2-Bromoacetyl)-4'-fluoromethanesulfonanilide収率 88.6%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

実験手順

3'-Acetyl-4'-fluoromethanesulfonanilide (32 g) was dissolved in 250 ml of acetic acid, then 22.1 g of bromine was dropped thereinto gradually at room temperature and the mixture was made to react at room temperature for 3 hours. The reaction mixture was added to ice water and the mixture-was extracted with ethyl acetate. The extract was washed with aqueous solution of sodium bicarbonate, then with water, dried and the solvent was evaporated therefrom followed by crystallizing from diisopropyl ether to give 38 g of 3'-(2-bromoacetyl)-4'-fluoromethanesulfonanilide, m.p. 110°-113° C.

後処理

  1. customgradually at room temperature
  2. customto react at room temperature for 3 hours
  3. extractionthe mixture-was extracted with ethyl acetate
  4. washThe extract was washed with aqueous solution of sodium bicarbonate
  5. dry with materialwith water, dried
  6. customthe solvent was evaporated
  7. customby crystallizing from diisopropyl ether

出典と根拠

ORDレコード
ord-7bc91113b29840a0856437345ad235fd
出典データセット
uspto-grants-1994_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05360822

反応ノート

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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