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Dimethyl malonate → HCID 10226524, 화합물

HRID 1797280
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인쇄 미리보기

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HRID 1797280 반응식
[H-].[Na+].[C:3]([O:10][CH3:11])(=[O:9])[CH2:4][C:5]([O:7][CH3:8])=[O:6].Br[CH2:13]/[CH:14]=[CH:15]/[Sn:16]([CH2:25][CH2:26][CH2:27][CH3:28])([CH2:21][CH2:22][CH2:23][CH3:24])[CH2:17][CH2:18][CH2:19][CH3:20]>CN(C=O)C>[CH2:25]([Sn:16]([CH2:21][CH2:22][CH2:23][CH3:24])([CH2:17][CH2:18][CH2:19][CH3:20])[CH2:15]/[CH:14]=[CH:13]/[CH:4]([C:3]([O:10][CH3:11])=[O:9])[C:5]([O:7][CH3:8])=[O:6])[CH2:26][CH2:27][CH3:28]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7943Dimethyl malonateHCID 24758Sodium hydrideHCID 10905679167288-95-1

생성물 1

HCID 10226524HCID 10226524, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
20 °C

실험 절차

Sodium hydride (75 mg) was added to a solution of dimethyl malonate (387 mg) in dry DMF (5 mL) at 0° C. [(1E)-3-bromoprop-1-enyl](tributyl)stannane (600 mg) was added to the reaction mixture after 10 min. The reaction mixture was stirred for 3 h at 20° C. and then quenched with saturated NH4Cl(aq.). Extraction with EtOAc and drying (MgSO4) of the organic phase gave, after concentration in vacuo, the crude product. Purification was done by chromatography eluting with petroleum ether/Et2O 12:1 to afford the title compound as a liquid.

후처리

  1. additionwas added to the reaction mixture after 10 min
  2. customquenched with saturated NH4Cl(aq.)
  3. extractionExtraction with EtOAc
  4. dry with materialdrying (MgSO4) of the organic phase
  5. customgave
  6. concentrationafter concentration in vacuo
  7. customPurification
  8. washeluting with petroleum ether/Et2O 12:1

출처 및 근거

ORD 기록
ord-9fb1341fe3c5408ca196de9ea8b1fa74
출처 데이터셋
uspto-grants-2006_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07034015B2

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