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Butyl bromide → 5-(1-Butyloxy)-2-nitrobenzyl alcohol

HRID 862664
ノート
印刷プレビュー

反応式

HRID 862664 の反応式
[OH:1][C:2]1[CH:3]=[CH:4][C:5]([N+:10]([O-:12])=[O:11])=[C:6]([CH:9]=1)[CH2:7][OH:8].C(=O)([O-])[O-].[K+].[K+].[CH2:19](Br)[CH2:20][CH2:21][CH3:22]>CN(C)C(=O)C>[CH2:19]([O:1][C:2]1[CH:3]=[CH:4][C:5]([N+:10]([O-:12])=[O:11])=[C:6]([CH:9]=1)[CH2:7][OH:8])[CH2:20][CH2:21][CH3:22]
参加物反応条件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 8002Butyl bromideHCID 11430Potassium CarbonateHCID 1089463-(Hydroxymethyl)-4-nitrophenol

生成物 1

HCID 540218025-(1-Butyloxy)-2-nitrobenzyl alcohol

試薬・触媒・溶媒 1

HCID 31374Dimethylacetamide溶媒

反応条件

温度
20 °C

実験手順

5.1 g (30 mmol) of 5-hydroxy-2-nitrobenzyl alcohol were stirred with 2.5 g (18 mmol) of potassium carbonate and 25 ml of N,N-dimethylacetamide at 70°-80° C. for 30 minutes. After cooling to 20° C., 3.9 ml (36 mmol) of 1-butylbromide were added dropwise and the mixture was stirred at 90° C. for 2 hours. After cooling, the reaction mixture was concentrated in vacuo, the residue was treated with water and the pH was brought to 7 with 2N HCl. The oil obtained crystallizes after about 30 minutes; the product was filtered off with suction, washed with water and dried; 6 g, melting point 47°-49° C.

後処理

  1. temperatureAfter cooling
  2. concentrationthe reaction mixture was concentrated in vacuo
  3. additionthe residue was treated with water
  4. customThe oil obtained
  5. customcrystallizes after about 30 minutes
  6. filtrationthe product was filtered off with suction
  7. washwashed with water
  8. customdried

出典と根拠

ORDレコード
ord-eab0bfe592004e65b31fefd351a48f31
出典データセット
uspto-grants-1998_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05719164

反応ノート

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