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2-Bromoethanol → HCID 12016698、化合物

HRID 1266949
ノート
印刷プレビュー

反応式

HRID 1266949 の反応式
[CH3:1][C:2]1[S:3][C:4]2[CH:10]=[C:9]([CH3:11])[CH:8]=[CH:7][C:5]=2[N:6]=1.[Br:12][CH2:13][CH2:14][OH:15]>C(OCC)(=O)C>[Br-:12].[OH:15][CH2:14][CH2:13][N+:6]1[C:5]2[CH:7]=[CH:8][C:9]([CH3:11])=[CH:10][C:4]=2[S:3][C:2]=1[CH3:1]
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 108982-BromoethanolHCID 762532,6-Dimethylbenzothiazole

生成物 1

HCID 12016698HCID 12016698、化合物収率 61%

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒

反応条件

温度
120 °C

実験手順

A solution of 2,6-dimethylbenzothiazole (13.0 g) and 2-bromoethanol (100 g) was stirred and heated in an oil bath to 120° C. for 96 hours. After cooling the reaction mixture to room temperature, adding ethyl acetate (150 ml) and stirring for 1 hour, the resultant solid was filtered and collected. The solid was then dissolved in methanol (150 ml) and charcoal (2 g) was added. The charcoal was removed by passing through a pad of Celite®. The solution was then concentrated to a small volume and triturated with acetone (200 ml). The solid was collected, washed with acetone (2×30 ml), ethyl acetate (2×30 ml) and dried in an oven under high vacuum at 50 C overnight to obtain 13.95 g (61%) of 4b.

後処理

  1. temperatureAfter cooling the reaction mixture to room temperature
  2. filtrationthe resultant solid was filtered
  3. customcollected
  4. dissolutionThe solid was then dissolved in methanol (150 ml)
  5. additioncharcoal (2 g) was added
  6. customThe charcoal was removed
  7. concentrationThe solution was then concentrated to a small volume
  8. customtriturated with acetone (200 ml)
  9. customThe solid was collected
  10. washwashed with acetone (2×30 ml), ethyl acetate (2×30 ml)
  11. customdried in an oven under high vacuum at 50 C overnight

出典と根拠

ORDレコード
ord-bca1855b717c479a8da8761348ec737a
出典データセット
uspto-grants-2003_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06551831B2

反応ノート

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