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2-Methoxyaniline → N-(4,5-dimethyl-1,3-dioxolan-2-ylmethyl)-2-methoxyaniline

HRID 28034
ノート
印刷プレビュー

反応式

HRID 28034 の反応式
[CH3:1][O:2][C:3]1[CH:9]=[CH:8][CH:7]=[CH:6][C:4]=1[NH2:5].C(=O)([O-])[O-].[Na+].[Na+].Br[CH2:17][CH:18]1[O:22][CH:21]([CH3:23])[CH:20]([CH3:24])[O:19]1>>[CH3:24][CH:20]1[CH:21]([CH3:23])[O:22][CH:18]([CH2:17][NH:5][C:4]2[CH:6]=[CH:7][CH:8]=[CH:9][C:3]=2[O:2][CH3:1])[O:19]1
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 3

HCID 70002-MethoxyanilineHCID 10340Sodium CarbonateHCID 128944572-Bromomethyl-4,5-dimethyl-1,3-dioxolane

生成物 1

HCID 23338386N-(4,5-dimethyl-1,3-dioxolan-2-ylmethyl)-2-methoxyaniline

反応条件

温度
100 °C

実験手順

2-Methoxyaniline (87 ml; 0.7 mole) and sodium carbonate (31.66 grams) were charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. 2-Bromomethyl-4,5-dimethyl-1,3-dioxolane (25 mls) was added and the reaction mixture was heated at a temperature of 100° C. for a period of about 4 hours. After this time the reaction mixture was filtered and additional sodium carbonate (5.00 grams) was added to the filtrate. The mixture was then distilled under reduced pressure to yield the desired product N-(4,5-dimethyl-1,3-dioxolan-2-ylmethyl)-2-methoxyaniline boiling at 125° to 128° C. at 0.1 mm of Hg pressure.

後処理

  1. customequipped with a mechanical stirrer
  2. temperaturethermometer and reflux condenser
  3. filtrationAfter this time the reaction mixture was filtered
  4. additionadditional sodium carbonate (5.00 grams) was added to the filtrate
  5. distillationThe mixture was then distilled under reduced pressure

出典と根拠

ORDレコード
ord-b450100da9fe427db4334b43432f4259
出典データセット
uspto-grants-1980_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04225335

反応ノート

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