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1,3-Dichloro-2-propanol → 1,3-Bis(2-(dimethylamino)ethylthio)-2-propanol

HRID 581645
ノート
印刷プレビュー

反応式

HRID 581645 の反応式
Cl.[CH3:2][N:3]([CH3:7])[CH2:4][CH2:5][SH:6].[OH-].[Na+].Cl[CH2:11][CH:12]([OH:15])[CH2:13]Cl>C(O)C>[CH3:2][N:3]([CH3:7])[CH2:4][CH2:5][S:6][CH2:11][CH:12]([OH:15])[CH2:13][S:6][CH2:5][CH2:4][N:3]([CH3:7])[CH3:2]
参加物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 72891,3-Dichloro-2-propanolHCID 14798Sodium HydroxideHCID 25798Captamine Hydrochloride

生成物 1

HCID 538484991,3-Bis(2-(dimethylamino)ethylthio)-2-propanol収率 85.6%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒2 回

実験手順

2-(Dimethylamino)ethanethiol hydrochloride (10.78 g, 78 mmole) was added portion-wise to a solution of sodium hydroxide (6.2 g, 155 mmole) in ethanol (40 mL) at 0° C. under nitrogen. A further portion of ethanol (20 mL) was added and the mixture stirred at this temperature for 10 minutes. 1,3-Dichloro-2-propanol (5.29 g, 41 mmole) was added dropwise. On completion of the addition, the reaction mixture was allowed to warm to room temperature and stirred for a further 2 hours. The precipitated solid was filtered off and the washed with ethanol. The filtrate was evaporated. The resulting oil was taken up into acetone, filtered and evaporated to give the desired product (8.90 g, 68%) as a pale yellow oil.

後処理

  1. additionOn completion of the addition
  2. stirringstirred for a further 2 hours
  3. filtrationThe precipitated solid was filtered off
  4. washthe washed with ethanol
  5. customThe filtrate was evaporated
  6. filtrationfiltered
  7. customevaporated

出典と根拠

ORDレコード
ord-7f7856a28c464f0c9a0eed16e605b3c2
出典データセット
uspto-grants-1999_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05922527

反応ノート

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