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Water → 2-Bromo-3-n-octylthiophene

HRID 713548
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HRID 713548 반응식
[CH2:1]([C:9]1[CH:13]=[CH:12][S:11][CH:10]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].C1C(=O)N([Br:21])C(=O)C1.O>CN(C=O)C>[Br:21][C:10]1[S:11][CH:12]=[CH:13][C:9]=1[CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 67184N-bromobutanimideHCID 5668523-Octylthiophene

생성물 1

HCID 107548542-Bromo-3-n-octylthiophene수율 89.9%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매2회

실험 절차

To a 250 mL of two-ported flask filled with 3-octylthiophene (10.00 g, 50.93 mmol) was added 60 mL of DMF. A solution of NBS (9.26 g, 52.03 mmol) in 60 mL of DMF was added dropwise in an iced saline bath. After addition was completed, the mixture was warmed to the room temperature and then stirred at this temperature overnight. The reaction was stopped and the resultant product was poured into 200 mL of water. The mixture was extracted with dichloromethane (60 mL×4). The organic phase was washed with aqueous potassium hydroxide solution (2 M, 100 mL), saturated saline (100 mL) and water (100 mL×2), successively. The organic phase was dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure. The resultant product was separated with chromatographic column, in which eluant was petroleum ether, to give a liquid as oil (12.60 g, yield: 89%).

후처리

  1. additionAfter addition
  2. extractionThe mixture was extracted with dichloromethane (60 mL×4)
  3. washThe organic phase was washed with aqueous potassium hydroxide solution (2 M, 100 mL), saturated saline (100 mL) and water (100 mL×2)
  4. dry with materialThe organic phase was dried over anhydrous sodium sulfate
  5. customThe solvent was removed under reduced pressure
  6. customThe resultant product was separated with chromatographic column, in which eluant

출처 및 근거

ORD 기록
ord-87c599d5515840b39461b1809f2ea70b
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09184315B2

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