Acetone → 2,4Dimethyl-3-acetyl-5-isopropyl pyrrole

HRID 1834411ノート

反応式

HRID 1834411 の反応式
[CH3:1][C:2]1[NH:3][CH:4]=[C:5]([CH3:10])[C:6]=1[C:7](=[O:9])[CH3:8].[CH3:11][C:12]([CH3:14])=O.O>Br.C(O)(=O)C>[CH3:1][C:2]1[NH:3][C:4]([CH:12]([CH3:14])[CH3:11])=[C:5]([CH3:10])[C:6]=1[C:7](=[O:9])[CH3:8]

参加物

6

反応物 3

HCID 180AcetoneHCID 962WaterHCID 15163Ketone, 2,4-dimethylpyrrol-3-yl methyl

生成物 1

HCID 28252872,4Dimethyl-3-acetyl-5-isopropyl pyrrole

試薬・触媒・溶媒 2

HCID 176Acetic Acid溶媒HCID 260Hydrogen Bromide溶媒

反応条件

温度
30 °C

実験手順

Anhydrous stannous bromide (5g) was stirred to solution in 20 ml of hydrogen bromide in acetic acid (30-32 %). 2,4-Dimethyl-3-acetyl-pyrrole (548 mg) was added and the mixture was warmed to dissolve this, then cooled to 30° C. Acetone(0.6 ml) was added and the solution was stirred at 35° C. for 21/2 hrs then poured into water at 10° C. The product was separated and washed with dilute hydrochloric acid then with water. It formed colourless micro-prisms (549 mg. 77%), m.p. 166°-167° C. or 173-174.5° C. after changing to cubes at about 136° C. For analysis it was recrystallized from aqueous ethanol as prismatic rods, m.p. 172° C.

後処理

  1. temperaturethe mixture was warmed
  2. dissolutionto dissolve this,
  3. customThe product was separated
  4. washwashed with dilute hydrochloric acid
  5. customIt formed colourless micro-prisms (549 mg. 77%), m.p. 166°-167° C. or 173-174.5° C.
  6. customafter changing to cubes at about 136° C
  7. customFor analysis it was recrystallized from aqueous ethanol as prismatic rods, m.p. 172° C.

出典と根拠

ORDレコード
ord-fd15fbc6001b447b9e1d033854dbe994
出典データセット
uspto-grants-1978_01
特許番号
US04070366

反応ノート

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