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Methyl 2-methyl-1-oxo-2,3-dihydro-1H-indene-2-carboxylate → Methyl 2-methyl-2,3-dihydro-1H-indene-2-carboxylate

HRID 547665
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HRID 547665 반응식
[CH3:1][C:2]1([C:12]([O:14][CH3:15])=[O:13])[CH2:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]1=O.[H][H]>C(O)(=O)C.OS(O)(=O)=O>[CH3:1][C:2]1([C:12]([O:14][CH3:15])=[O:13])[CH2:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3]1
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5

반응물 2

HCID 12522314Methyl 2-methyl-1-oxo-2,3-dihydro-1H-indene-2-carboxylateHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 57565328Methyl 2-methyl-2,3-dihydro-1H-indene-2-carboxylate

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 1118Sulfuric Acid용매

실험 절차

A solution of the methyl 2-methyl-1-oxo-2,3-dihydro-1H-indene-2-carboxylate (2.04 g, 9.99 mmol) in glacial acetic acid (22 mL) and concentrated H2SO4 (2 mL) was hydrogenated on a Parr apparatus under 50 psi of hydrogen using 10% palladium on carbon (50% H2O, 0.200 g) as the catalyst. After 4 hours the reaction was filtered to remove the catalyst and washed 2× methanol, then concentrated to remove most of the acetic acid. The residue was neutralized using saturated Na2CO3 and the organics extracted twice with 25 mL ethyl acetate, then the combined organics washed with brine, dried (Na2SO4), filtered and concentrated to 2.0 g of methyl 2-methyl-2,3-dihydro-1H-indene-2-carboxylate.

후처리

  1. filtrationAfter 4 hours the reaction was filtered
  2. customto remove the catalyst
  3. washwashed 2× methanol
  4. concentrationconcentrated
  5. customto remove most of the acetic acid
  6. extractionthe organics extracted twice with 25 mL ethyl acetate
  7. washthe combined organics washed with brine
  8. dry with materialdried (Na2SO4)
  9. filtrationfiltered
  10. concentrationconcentrated to 2.0 g of methyl 2-methyl-2,3-dihydro-1H-indene-2-carboxylate

출처 및 근거

ORD 기록
ord-51d3487e014240dba915a8efcdb4f4a2
출처 데이터셋
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07939528B2

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