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Homovanillic Acid → HCID 22600136, 화합물

HRID 1760031
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HRID 1760031 반응식
C([O-])([O-])=O.[Cs+].[Cs+].[C:7]([OH:19])(=[O:18])[CH2:8][C:9]1[CH:17]=[CH:16][C:14]([OH:15])=[C:11]([O:12][CH3:13])[CH:10]=1.[CH:20]1[CH:25]=[CH:24][C:23]([CH2:26]Br)=[CH:22][CH:21]=1>CC#N>[CH2:26]([O:15][C:14]1[CH:16]=[CH:17][C:9]([CH2:8][C:7]([O:19][CH2:8][C:9]2[CH:17]=[CH:16][CH:14]=[CH:11][CH:10]=2)=[O:18])=[CH:10][C:11]=1[O:12][CH3:13])[C:23]1[CH:24]=[CH:25][CH:20]=[CH:21][CH:22]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1738Homovanillic AcidHCID 7498Benzyl BromideHCID 10796Cesium carbonate

생성물 1

HCID 22600136HCID 22600136, 화합물

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

Cs2CO3 (17.88 g; 54.9 mmol) was added to a solution of homovanillic acid (2.0 g; 11 mmol) in CH3CN, whereafter BnBr (4.3 g; 24.15 mmol) was added dropwise over 10 minutes. The mixture was refluxed overnight, filtered through Hyflo and concentrated. The resulting mixture was dissolved in EtOAc (100 mL), water (30 mL) was added, and the aqueous layer was separated. The organic phase was washed with citric acid solution (5%, 1×20 mL) and brine, dried (Na2SO4), and evaporated to yield 4.25 g (quant.) of the sub-title compound.

후처리

  1. additionwas added dropwise over 10 minutes
  2. temperatureThe mixture was refluxed overnight
  3. filtrationfiltered through Hyflo
  4. concentrationconcentrated
  5. dissolutionThe resulting mixture was dissolved in EtOAc (100 mL)
  6. additionwater (30 mL) was added
  7. customthe aqueous layer was separated
  8. washThe organic phase was washed with citric acid solution (5%, 1×20 mL) and brine
  9. dry with materialdried (Na2SO4)
  10. customevaporated

출처 및 근거

ORD 기록
ord-5aeaad112e1742ccaf56452ba636b6f2
출처 데이터셋
uspto-grants-2005_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06838478B2

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