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Dimethylformamide → HCID 22458192, 화합물

HRID 2184849
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HRID 2184849 반응식
[F:1][C:2]([F:17])([F:16])[O:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[N:10]1[CH2:15][CH2:14][NH:13][CH2:12][CH2:11]1.Br[CH2:19][CH2:20][OH:21].CCN(C(C)C)C(C)C.CN(C=O)C>O>[OH:21][CH2:20][CH2:19][N:13]1[CH2:14][CH2:15][N:10]([C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[O:3][C:2]([F:1])([F:16])[F:17])[CH2:11][CH2:12]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 6228DimethylformamideHCID 108982-BromoethanolHCID 81531DiisopropylethylamineHCID 107529251-(2-Trifluoromethoxyphenyl)piperazine

생성물 1

HCID 22458192HCID 22458192, 화합물수율 63%

시약·촉매·용매 1

HCID 962Water용매

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온도
65 °C

실험 절차

A stirred mixture of 1.23 g of 1-(2-trifluoromethoxyphenyl)piperazine, 0.73 mL of 97% 2-bromoethanol, 1.25 mL of DIPEA and 4 mL of DMF was heated at 65° C. for 6 h. After cooling to r.t., the mixture was diluted with H2O (50 mL) and extracted with CH2Cl2 (3×30 mL). The organic layer was dried (anhydrous Na2SO4) and evaporated to dryness in vacuo. The residue was purified by flash chromatography (CH2Cl2-MeOH 100:1.5) affording 0.911 g (63%) of the title compound.

후처리

  1. temperatureAfter cooling to r.t.
  2. extractionextracted with CH2Cl2 (3×30 mL)
  3. dry with materialThe organic layer was dried (anhydrous Na2SO4)
  4. customevaporated to dryness in vacuo
  5. customThe residue was purified by flash chromatography (CH2Cl2-MeOH 100:1.5)

출처 및 근거

ORD 기록
ord-c95f844559df41358d24c5cb20c8eb2d
출처 데이터셋
uspto-grants-2002_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06399614B1

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