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Iodoethane → Methyl 3-ethoxy-4-methoxybenzoate

HRID 1595734
ノート
印刷プレビュー

反応式

HRID 1595734 の反応式
[OH:1][C:2]1[CH:3]=[C:4]([CH:9]=[CH:10][C:11]=1[O:12][CH3:13])[C:5]([O:7][CH3:8])=[O:6].C(=O)([O-])[O-].[K+].[K+].[CH2:20](I)[CH3:21]>CN(C)C=O>[CH2:20]([O:1][C:2]1[CH:3]=[C:4]([CH:9]=[CH:10][C:11]=1[O:12][CH3:13])[C:5]([O:7][CH3:8])=[O:6])[CH3:21]
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 6340Iodoethane2 回HCID 11430Potassium Carbonate2 回HCID 4056967Methyl 3-hydroxy-4-methoxybenzoate

生成物 1

HCID 10536413Methyl 3-ethoxy-4-methoxybenzoate収率 55.4%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
100 °C

実験手順

A mixture of 24.3 g (134 mmol) of methyl 3-hydroxy-4-methoxybenzoate, 36.8 g (267 mmol) of anhyd potassium carbonate and 31.4 g (201 mmol) of ethyl iodide in 500 mL of dimethylformamide was stirred at 100° C. for 5.5 h. An additional amount of ethyl iodide (31.4 g) and potassium carbonate (18.4 g) was added and heating was continued for 2 h more. The reaction was filtered and volatile material was removed from the filtrate in vacuo. The residue was slurried with water and filtered to collect the product which was washed with water and dried. Recrystallization from heptane gave 15.6 g of methyl 3-ethoxy-4-methoxybenzoate as white crystals: mass spectrum (electrospray, m/e): M+H 210.9.

後処理

  1. temperatureheating
  2. waitwas continued for 2 h
  3. filtrationThe reaction was filtered
  4. customvolatile material was removed from the filtrate in vacuo
  5. filtrationfiltered
  6. customto collect the product which
  7. washwas washed with water
  8. customdried
  9. customRecrystallization from heptane

出典と根拠

ORDレコード
ord-adcad9f1df574ced8df58898487fea75
出典データセット
uspto-grants-2001_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06288082B1

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート