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2-Bromoethanol → HCID 12016698, 화합물

HRID 1266949
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HRID 1266949 반응식
[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]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 108982-BromoethanolHCID 762532,6-Dimethylbenzothiazole

생성물 1

HCID 12016698HCID 12016698, 화합물수율 61%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

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온도
120 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-bca1855b717c479a8da8761348ec737a
출처 데이터셋
uspto-grants-2003_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06551831B2

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