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Water → 4-Anilinophenyl crotonate

HRID 26044
ノート
印刷プレビュー

反応式

HRID 26044 の反応式
[C:1](Cl)(=[O:5])/[CH:2]=[CH:3]/[CH3:4].[Na].[NH:8]([C:15]1[CH:20]=[CH:19][C:18]([OH:21])=[CH:17][CH:16]=1)[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1.O>C1C=CC=CC=1.[OH-].[Na+].C(O)C>[C:1]([O:21][C:18]1[CH:17]=[CH:16][C:15]([NH:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)=[CH:20][CH:19]=1)(=[O:5])/[CH:2]=[CH:3]/[CH3:4]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 962WaterHCID 312084-Hydroxydiphenylamine2 回HCID 643131trans-Crotonyl chlorideHCID 5360545Sodium

生成物 1

HCID 211636064-Anilinophenyl crotonate

試薬・触媒・溶媒 3

HCID 241Benzene溶媒
HCID 702
Ethanol
溶媒
HCID 14798Sodium Hydroxide溶媒

実験手順

4-Anilinophenyl crotonate was prepared by adding a solution of 11.5 grams of crotonyl chloride in 50 milliliters of benzene to a solution of the sodium salt of 4-anilinophenol which was prepared by dissolving 18.5 grams of 4-anilinophenol in a solution of 4 grams of sodium hydroxide in 100 milliliters of ethanol. The addition was accomplished in 30 minutes and the reaction mixture was stirred for one hour. The mixture was then poured into 150 milliliters of water. The organic layer was separated, washed three times with 10 percent sodium hydroxide solution and once with water, dried over anhydrous sodium sulfate, then allowed to evaporate. The residue was recrystallized from hexane yielding 13.3 grams of product which melted at 73°-76° C.

後処理

  1. customwas prepared
  2. additionThe addition
  3. customThe organic layer was separated
  4. washwashed three times with 10 percent sodium hydroxide solution
  5. dry with materialonce with water, dried over anhydrous sodium sulfate
  6. customto evaporate
  7. customThe residue was recrystallized from hexane yielding 13.3 grams of product which melted at 73°-76° C.

出典と根拠

ORDレコード
ord-3e50ab561b124247a9b9c228a91b812e
出典データセット
uspto-grants-1979_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04147880

反応ノート

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