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Allyl bromide → HCID 10586690、化合物

HRID 1084942
ノート
印刷プレビュー

反応式

HRID 1084942 の反応式
C(=O)([O-])[O-].[K+].[K+].[CH2:7](Br)[CH:8]=[CH2:9].[OH:11][C:12]1[CH:21]=[C:20]([NH:22][C:23]([CH3:25])=[O:24])[CH:19]=[CH:18][C:13]=1[C:14]([O:16][CH3:17])=[O:15]>[Cl-].C([N+](CCCC)(CCCC)CCCC)C1C=CC=CC=1.C(#N)C>[CH2:7]([O:11][C:12]1[CH:21]=[C:20]([NH:22][C:23]([CH3:25])=[O:24])[CH:19]=[CH:18][C:13]=1[C:14]([O:16][CH3:17])=[O:15])[CH:8]=[CH2:9]
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 3

HCID 7841Allyl bromideHCID 11430Potassium CarbonateHCID 77719Methyl 4-acetamidosalicylate

生成物 1

HCID 10586690HCID 10586690、化合物

試薬・触媒・溶媒 2

HCID 159952Benzyltributylammonium chloride触媒HCID 6342Acetonitrile溶媒

実験手順

138 g of potassium carbonate, 16.5 g of benzyltributylammonium chloride, 650 ml of acetonitrile and 133 g of allyl bromide were introduced into a 2-liter round-bottomed flask and 209 g of ground methyl 2-hydroxy-4-acetaminobenzoate were then added in small amounts. The contents were heated under reflux for 11 hours, a part of the acetonitrile was then distilled off and the residue was taken up with water. The precipitate formed was drained, washed with water and dried in an oven at 50° C.

後処理

  1. temperatureThe contents were heated
  2. temperatureunder reflux for 11 hours
  3. distillationa part of the acetonitrile was then distilled off
  4. customThe precipitate formed
  5. washwashed with water
  6. customdried in an oven at 50° C.

出典と根拠

ORDレコード
ord-81098b8e6f994524a06924cf1311afc9
出典データセット
uspto-grants-1991_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05006570

反応ノート

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