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Methyl 4-cyano-2-fluorobenzoate → Methyl 4-(aminomethyl)-2-fluorobenzoate

HRID 911628
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HRID 911628 반응식
[C:1]([C:3]1[CH:12]=[CH:11][C:6]([C:7]([O:9][CH3:10])=[O:8])=[C:5]([F:13])[CH:4]=1)#[N:2]>C(O)C.C(O)(=O)C.O.[Pd]>[NH2:2][CH2:1][C:3]1[CH:12]=[CH:11][C:6]([C:7]([O:9][CH3:10])=[O:8])=[C:5]([F:13])[CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 1

HCID 15278726Methyl 4-cyano-2-fluorobenzoate

생성물 1

HCID 57572260Methyl 4-(aminomethyl)-2-fluorobenzoate수율 59%

시약·촉매·용매 4

HCID 23938Palladium촉매HCID 176Acetic Acid용매HCID 702Ethanol용매HCID 962Water용매

실험 절차

Combine a solution of methyl 4-cyano-2-fluoro-benzoate (1 g, 5.58 mmol) in absolute ethanol (42 mL) and acetic acid (1.9 mL) with a mixture of 10% Pd/C (Degussa type E101, 0.17 g, 0.078 mmol) in water (15.6 mL) at room temperature under nitrogen. Purge with nitrogen and then with hydrogen at 55 psi and stir for 1 h. Purge the reaction with nitrogen, filter through Celite® and wash the filter cake with ethanol (100 mL), THF (100 mL) and isopropanol (100 mL). Concentrate in vacuo and purify by SCX chromatography and then chromatography on silica gel (40 g RediSep® column) eluting with dichloromethane/2M ammonia in methanol (99:1 to 9:1 gradient over 30 min; 35 mL/min) to afford the desired intermediate as a white solid (0.602 g, 59%).

후처리

  1. customPurge with nitrogen
  2. customPurge
  3. customthe reaction with nitrogen
  4. filtrationfilter through Celite®
  5. washwash the filter cake with ethanol (100 mL), THF (100 mL) and isopropanol (100 mL)
  6. concentrationConcentrate in vacuo
  7. custompurify by SCX chromatography
  8. washchromatography on silica gel (40 g RediSep® column) eluting with dichloromethane/2M ammonia in methanol (99:1 to 9:1 gradient over 30 min; 35 mL/min)

출처 및 근거

ORD 기록
ord-b91aa744385a49ab9cb548960eba3105
출처 데이터셋
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08022062B2

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