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Methyl 5-(benzyloxycarbonyl)-2,4-dimethyl-3-pyrrolepropionate → Methyl 2,4-dimethyl-3-pyrrolepropionate

HRID 1188018
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HRID 1188018 반응식
C(OC([C:11]1[NH:15][C:14]([CH3:16])=[C:13]([CH2:17][CH2:18][C:19]([O:21][CH3:22])=[O:20])[C:12]=1[CH3:23])=O)C1C=CC=CC=1>CC(C)=O.[Pd]>[CH3:22][O:21][C:19]([CH2:18][CH2:17][C:13]1[C:12]([CH3:23])=[CH:11][NH:15][C:14]=1[CH3:16])=[O:20]
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참가 물질

4

반응물 1

HCID 657433Methyl 5-(benzyloxycarbonyl)-2,4-dimethyl-3-pyrrolepropionate

생성물 1

HCID 10559312Methyl 2,4-dimethyl-3-pyrrolepropionate수율 90.1%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 180Acetone용매

실험 절차

Methyl 5-(benzyloxycarbonyl)-2,4-dimethyl-3-pyrrolepropionate (3.1 g, 9.8 mmol) was dissolved in acetone (100 mL). This solution was added with 10% Pd—C, and stirred at room temperature under hydrogen gas. When the starting material disappeared, the reaction mixture was filtered, and the filtrate was distilled under reduced pressure. The residue was added with trifluoroacetic acid (10 mL), and heated at 40° C. for 10 minutes under an argon flow. The reaction mixture was added with chloroform, and washed once with water, and the aqueous layer was extracted twice with chloroform. The organic phases were combined, washed once with aqueous Na2CO3 and once with water, dried over anhydrous Na2SO4, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (developing solvent: CH2Cl2) to obtain the target compound as brown liquid (1.6 g, yield: 90%).

후처리

  1. filtrationthe reaction mixture was filtered
  2. distillationthe filtrate was distilled under reduced pressure
  3. additionThe residue was added with trifluoroacetic acid (10 mL)
  4. temperatureheated at 40° C. for 10 minutes under an argon flow
  5. additionThe reaction mixture was added with chloroform
  6. washwashed once with water
  7. extractionthe aqueous layer was extracted twice with chloroform
  8. washwashed once with aqueous Na2CO3 and once with water
  9. dry with materialdried over anhydrous Na2SO4
  10. concentrationconcentrated under reduced pressure
  11. customThe residue was purified by silica gel column chromatography (developing solvent: CH2Cl2)

출처 및 근거

ORD 기록
ord-7d1069f2f2a14e0f88456f3c0d9c5ac8
출처 데이터셋
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08673957B2

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