Methyl acetoacetate → HCID 58762397, 화합물

HRID 1453318

반응식

HRID 1453318 반응식
[Li+].CC([N-]C(C)C)C.[C:9]([O:15][CH3:16])(=[O:14])[CH2:10][C:11]([CH3:13])=[O:12].[CH:17]1([C:22](=[O:36])[CH2:23][CH2:24][C:25]#[C:26][C:27]2[CH:32]=[C:31]([CH3:33])[C:30]([OH:34])=[CH:29][C:28]=2[CH3:35])[CH2:21][CH2:20][CH2:19][CH2:18]1>C1COCC1>[CH3:16][O:15][C:9](=[O:14])[CH2:10][C:11](=[O:12])[CH2:13][C:22]([CH:17]1[CH2:21][CH2:20][CH2:19][CH2:18]1)([OH:36])[CH2:23][CH2:24][C:25]#[C:26][C:27]1[CH:32]=[C:31]([CH3:33])[C:30]([OH:34])=[CH:29][C:28]=1[CH3:35]

참가 물질

5

실험 절차

To a freshly prepared solution of LDA (1 M, 2.2 mL, 2.2 mmol) cooled to 0° C. was added methyl acetoacetate (0.12 mL, 1.1 mmol) dissolved in THF (1 mL). After stirring for 30 minutes, 1-cyclopentyl-5-(4-hydroxy-2,5-dimethyl-phenyl)-pent-4-yn-1-one (0.10 g, 0.37 mmol) from Step 1 above dissolved in THF (1 mL) was added. The reaction was stirred for 1Hour, and then warmed to room temperature. After quenching with 10 mL saturated ammonium chloride, the layers were separated. The aqueous layer was extracted with 2×15 mL CH2Cl2, and the organic layers were combined. After drying over Na2SO4, and filtering to remove the solids, the mother liquor was concentrated to an oil. Flash chromatography of the oil gave the desired product (69 mg, 48% yield).

후처리

  1. additionwas added
  2. stirringThe reaction was stirred for 1Hour
  3. customAfter quenching with 10 mL saturated ammonium chloride
  4. customthe layers were separated
  5. extractionThe aqueous layer was extracted with 2×15 mL CH2Cl2
  6. dry with materialAfter drying over Na2SO4
  7. filtrationfiltering
  8. customto remove the solids
  9. concentrationthe mother liquor was concentrated to an oil

출처 및 근거

ORD 기록
ord-def68bf565c74f419f2ccceeab3b2ce1
출처 데이터셋
uspto-grants-2009_01
특허 번호
US07473790B2

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