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Methyl 3-bromo-4-ethylbenzoate → HCID 57935767, 화합물

HRID 1434576
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HRID 1434576 반응식
Br[C:2]1[CH:3]=[C:4]([CH:9]=[CH:10][C:11]=1[CH2:12][CH3:13])[C:5]([O:7][CH3:8])=[O:6].[Cu][C:15]#[N:16]>CN1C(=O)CCC1.O>[C:15]([C:2]1[CH:3]=[C:4]([CH:9]=[CH:10][C:11]=1[CH2:12][CH3:13])[C:5]([O:7][CH3:8])=[O:6])#[N:16]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 13877473Methyl 3-bromo-4-ethylbenzoateHCID 178418546HCID 178418546, 화합물

생성물 1

HCID 57935767HCID 57935767, 화합물수율 48.8%

시약·촉매·용매 2

HCID 962Water용매HCID 13387N-methyl-2-pyrrolidone용매

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온도
20 °C

실험 절차

Methyl 3-bromo-4-ethyl-benzoate (D44) (5 g) in NMP (180 mL) was treated with copper (I) cyanide (3.69 g). The mixture was then heated at reflux for 5 h, under argon. After cooling to 20° C. the reaction mixture was diluted with water, then filtered through kieselguhr, washing well with water and EtOAc. The organic layer was washed with water, brine and dried over MgSO4. The solvent was evaporated to dryness in vacuo and the residue was purified by chromatography on silica eluting with EtOAc-Hexane (1:9) to give the title compound (1.9 g) 1H NMR (CDCl3) δ 1.33 (3H, t), 2.94 (2H, q), 3.94 (3H, s), 7.43 (1H, d), 8.17 (1H, dd), 8.28 (1H, d).

후처리

  1. temperatureThe mixture was then heated
  2. temperatureat reflux for 5 h, under argon
  3. filtrationfiltered through kieselguhr
  4. washwashing well with water and EtOAc
  5. washThe organic layer was washed with water, brine
  6. dry with materialdried over MgSO4
  7. customThe solvent was evaporated to dryness in vacuo
  8. customthe residue was purified by chromatography on silica eluting with EtOAc-Hexane (1:9)

출처 및 근거

ORD 기록
ord-c03fb10769df4fdc886e65121664c9c9
출처 데이터셋
uspto-grants-2009_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07615550B2

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