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Dimethylamine → 2-(2-Methylpropoxy)benzoic acid

HRID 2225955
ノート
印刷プレビュー

反応式

HRID 2225955 の反応式
CNC.Cl[C:5]1[CH:13]=[CH:12][CH:11]=[CH:10][C:6]=1[C:7]([OH:9])=[O:8]>C(O)C(C)C>[CH2:7]([O:8][C:5]1[CH:13]=[CH:12][CH:11]=[CH:10][C:6]=1[C:7]([OH:9])=[O:8])[CH:6]([CH3:10])[CH3:5]
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

4

反応物 2

HCID 674DimethylamineHCID 83742-Chlorobenzoic Acid

生成物 1

HCID 149555242-(2-Methylpropoxy)benzoic acid収率 141.4%

試薬・触媒・溶媒 1

HCID 6560Isobutanol溶媒2 回

反応条件

温度
100 °C

実験手順

In a pressure-resistant sealed vessel, were dissolved 1.14 g of o-chlorobenzoic acid (7.3 mM) and 0.18 g of cuprous chloride (1.8 mM) in 5 g of an isobutyl alcohol solution containing 20% dimethylamine (about 6.0 ml) prior to addition of isobutyl alcohol to a total volume of 50 ml, followed by heating to 100° C. as in Example 4. The reaction mixture solution was analyzed periodically over time by GC-MSE1 in the same manner as in Example 4, in order to follow the progress of the reaction. As a result, 20 hours later, the completion of the reaction was confirmed. Effecting the subsequent process in the same manner as in Example 4, 1.0 g of 2-isobutoxybenzoic acid was obtained (yield of 70.6%). The ester of the above product (3%) and benzoic acid (5%) were also obtained as the byproducts, which were confirmed by 1H-NMR and GC-MSE1.

後処理

  1. customthe progress of the reaction
  2. customAs a result, 20 hours

出典と根拠

ORDレコード
ord-9f3e5786e1ed4b6ba3f622ea336392d3
出典データセット
uspto-grants-1994_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05344968

反応ノート

読み込み中…

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