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(2-thioxo-1,3-benzothiazol-3(2H)-yl)acetic acid → Methyl (2-sulfanylidene-1,3-benzothiazol-3(2H)-yl)acetate

HRID 543892
ノート
印刷プレビュー

反応式

HRID 543892 の反応式
[C:1]([CH2:4][N:5]1[C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][C:8]=2[S:7][C:6]1=[S:14])([OH:3])=[O:2].[C:15](=O)(O)[O-].[Na+]>CO>[S:14]=[C:6]1[N:5]([CH2:4][C:1]([O:3][CH3:15])=[O:2])[C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][C:8]=2[S:7]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 2

HCID 351524(2-thioxo-1,3-benzothiazol-3(2H)-yl)acetic acidHCID 516892Sodium Bicarbonate

生成物 1

HCID 13034583Methyl (2-sulfanylidene-1,3-benzothiazol-3(2H)-yl)acetate収率 94%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

反応条件

温度
0 °C

実験手順

To a stirred solution containing 45.1 g (0.2 mol) of 3-(carboxymethyl) benzothiazoline-2-thione in 600 ml of methyl alcohol, 142.0 g (1.0 mol) of boron trifluoride ether complex was added in one portion. An exothermic reaction set in causing a temperature rise from 20° to 37° C. The stirred solution was heated at reflux for 24 hours and then cooled to 0° C. After cooling, 1400 ml of 10% aqueous sodium bicarbonate was slowly added (foaming observed) at 0°-10° C. until pH 8 was obtained. After stirring at 0°-10° C. for one hour, the solid was collected by filtration, washed with water until neutral to litmus and air-dried at 25°-30° C. The product, 2-thioxo-3(2H)-benzothiazoleacetic acid, methyl ester was obtained in 94% yield, m.p. 127°-128° C.

後処理

  1. additionwas added in one portion
  2. customAn exothermic reaction
  3. customfrom 20° to 37° C
  4. temperatureThe stirred solution was heated
  5. temperatureat reflux for 24 hours
  6. temperatureAfter cooling
  7. customwas obtained
  8. filtrationthe solid was collected by filtration
  9. washwashed with water until neutral to litmus and
  10. customair-dried at 25°-30° C

出典と根拠

ORDレコード
ord-8fd6b2cec0644f53ba68ebf61a3cf82f
出典データセット
uspto-grants-1984_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04447618

反応ノート

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