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Hydrochloric Acid → 4-Cinnamoylamino-3-methylbenzoic acid

HRID 232702
ノート
印刷プレビュー

反応式

HRID 232702 の反応式
C(=O)([O-])[O-].[K+].[K+].[NH2:7][C:8]1[CH:16]=[CH:15][C:11]([C:12]([OH:14])=[O:13])=[CH:10][C:9]=1[CH3:17].[C:18](Cl)(=[O:27])[CH:19]=[CH:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1.Cl>CC(C)=O.O>[C:18]([NH:7][C:8]1[CH:16]=[CH:15][C:11]([C:12]([OH:14])=[O:13])=[CH:10][C:9]=1[CH3:17])(=[O:27])[CH:19]=[CH:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 313Hydrochloric AcidHCID 11430Potassium CarbonateHCID 660233-Phenylprop-2-enoyl chlorideHCID 755984-Amino-3-methylbenzoic acid

生成物 1

HCID 538459644-Cinnamoylamino-3-methylbenzoic acid収率 51.9%

試薬・触媒・溶媒 2

HCID 180Acetone溶媒
2 回
HCID 962Water溶媒

実験手順

8.2 g of potassium carbonate was added to a suspension of 3.0 g of 4-amino-3-methylbenzoic acid in 60 ml of acetone and 60 ml of water. Thereto was dropwise added, with ice-cooling, a solution of 4.0 g of cinnamoyl chloride in 30 ml of acetone. The mixture was stirred at the same temperature for 30 minutes to give rise to a reaction. The reaction mixture was poured into ice water, and the mixture was made acidic with concentrated hydrochloric acid. The resulting precipitate was collected by filtration, washed with water, and recrystallized from methanol to obtain 2.9 g of 4-cinnamoylamino-3-methylbenzoic acid as a white powder.

後処理

  1. additionThereto was dropwise added, with ice-
  2. temperaturecooling
  3. customto give rise
  4. customto a reaction
  5. filtrationThe resulting precipitate was collected by filtration
  6. washwashed with water
  7. customrecrystallized from methanol

出典と根拠

ORDレコード
ord-9c61d25f4f40453683cf50dca277638d
出典データセット
uspto-grants-1997_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05591751

反応ノート

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