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Methylamine → N-(4,4,6,6-tetramethyl-1,3-dithian-2-ylmethyl)methylamine

HRID 127142
ノート
印刷プレビュー

反応式

HRID 127142 の反応式
Cl[CH2:2][CH:3]1[S:8][C:7]([CH3:10])([CH3:9])[CH2:6][C:5]([CH3:12])([CH3:11])[S:4]1.[OH-].[Na+].[CH3:15][NH2:16]>>[CH3:11][C:5]1([CH3:12])[CH2:6][C:7]([CH3:10])([CH3:9])[S:8][CH:3]([CH2:2][NH:16][CH3:15])[S:4]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 6329MethylamineHCID 14798Sodium HydroxideHCID 202861232-Chloromethyl-4,4,6,6-tetramethyl-1,3-dithiane

生成物 1

HCID 53834633N-(4,4,6,6-tetramethyl-1,3-dithian-2-ylmethyl)methylamine

反応条件

温度
100 °C

実験手順

2-Chloromethyl-4,4,6,6-tetramethyl-1,3-dithiane (60 grams) and 40% aqueous methylamine (160 ml) are charged into a pressure vessel and heated, with agitation, at a temperature of about 100° C. for a period of about 16 hours under autogeneous pressure. At the end of this period, the reaction mixture is cooled to room temperature and 16 grams of sodium hydroxide are added. The resulting mixture is extracted with methylene chloride. The extract is dried, then stripped of solvent to yield the desired product N-(4,4,6,6-tetramethyl-1,3-dithian-2-ylmethyl)methylamine.

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

後処理

  1. temperatureAt the end of this period, the reaction mixture is cooled to room temperature
  2. extractionThe resulting mixture is extracted with methylene chloride
  3. customThe extract is dried

出典と根拠

ORDレコード
ord-f8901deb3e4f4b5a849cab9c052adb11
出典データセット
uspto-grants-1981_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04255182

反応ノート

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