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Chloroacetyl chloride → 4-(2-chloroacetyl)-1H-pyrrole-2-carbaldehyde

HRID 1494415
ノート
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反応式

HRID 1494415 の反応式
[NH:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH:6]=[O:7].[Cl-].[Al+3].[Cl-].[Cl-].[Cl:12][CH2:13][C:14](Cl)=[O:15]>ClC(Cl)C>[CH:6]([C:2]1[NH:1][CH:5]=[C:4]([C:14](=[O:15])[CH2:13][Cl:12])[CH:3]=1)=[O:7]
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 6577Chloroacetyl chlorideHCID 13854Pyrrole-2-carboxaldehydeHCID 6451240Aluminum(III) Chloride

生成物 1

HCID 27634524-(2-chloroacetyl)-1H-pyrrole-2-carbaldehyde収率 94%

試薬・触媒・溶媒 1

HCID 63651,1-Dichloroethane溶媒

実験手順

A mixture of 35 g (0.37 mole) pyrrole-2-carboxaldehyde in 325 ml dichloroethane was stirred under nitrogen in a three-necked, one-liter, round-bottomed flask fitted with an overhead stirrer and addition funnel. To this was added, in portions over a one-hour period, 294 g (2.21 mole) aluminum chloride. After the addition was completed, the mixture was stirred at room temperature for 10 minutes, then 124.7 g (88 ml, 1.10 mole) of chloroacetyl chloride was added dropwise over a one-hour period. The mixture was stirred at room temperature for 16 hours, then carefully poured into one liter of ice-water. The resulting precipitate (purple) was collected, washed well with water, and dried in vacuo. The dry solid was placed in a Soxhlet extractor and extracted with ethyl acetate for 20 hours. Concentration of the ethyl acetate solution afforded 59.4 g (94%) of the title compound as a yellow-green solid; m.p. 178°-179° C. This intermediate was used immediately in the next step. An analytical sample could be prepared by recrystallization from acetone.

後処理

  1. customfitted with an overhead stirrer and addition funnel
  2. additionTo this was added, in portions over a one-hour period
  3. additionAfter the addition
  4. stirringthe mixture was stirred at room temperature for 10 minutes
  5. stirringThe mixture was stirred at room temperature for 16 hours
  6. customThe resulting precipitate (purple) was collected
  7. washwashed well with water
  8. customdried in vacuo
  9. extractionextracted with ethyl acetate for 20 hours

出典と根拠

ORDレコード
ord-c1002e677caa44f3a8840ae634ffae5f
出典データセット
uspto-grants-1991_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05026715

反応ノート

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