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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → 2-(3-Oxo-cyclohexyl)-malonic acid dibenzyl ester

HRID 352213
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HRID 352213 반응식
[H-].[H-].[H-].[H-].[Li+].[Al+3].[Na].[C:8]([O:14][CH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)(=[O:13])[CH2:9][C:10]([O-:12])=[O:11].[H-].[Na+].[C:24]1(=[O:30])[CH2:29][CH2:28][CH2:27][CH:26]=[CH:25]1.Cl>C1COCC1>[CH2:15]([O:14][C:8](=[O:13])[CH:9]([CH:26]1[CH2:27][CH2:28][CH2:29][C:24](=[O:30])[CH2:25]1)[C:10]([O:12][CH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)=[O:11])[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

8

반응물 6

HCID 313Hydrochloric AcidHCID 135942-Cyclohexen-1-oneHCID 24758Sodium hydrideHCID 5360545SodiumHCID 21226445Aluminium lithium hydrideHCID 22247814Benzyl malonate

생성물 1

HCID 66361702-(3-Oxo-cyclohexyl)-malonic acid dibenzyl ester
수율 141.7%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매3회

실험 절차

To a solution of LiAlH4 (6 mL, 6 mmol) under N2 at 0° C. was added a solution of (S)-1,1′-binaphthol (3.43 g, 12 mmol) in THF (48 mL) and stirred for 30 min. The reaction was warmed to RT. To this was added a solution of sodium salt benzyl malonate in THF which was prepared by reacting benzyl malonate (14.99 mL, 60 mmol), NaH (60% by wt., 0.216 g, 5.4 mmol), and THF (60 mL) until all bubbling ceased. Next, cyclohexenone (5.82 mL, 60 mmol) and dibenzlmalonate (1.35 mL, 5.4 mmol) were added and the reaction mixture was stirred overnight. 1.0 N HCl was added and extracted with EtOAc (3×). The combined EtOAc layers were washed (brine), dried (MgSO4), filtered, and concentrated. Flash chromatography (silica gel, acetone/hexanes gradient) gave the title compound (16.17 g, 71%). Mass Spectrum (FIA) (m/z) 381.3 [M+1].

후처리

  1. customwas prepared
  2. stirringthe reaction mixture was stirred overnight
  3. extractionextracted with EtOAc (3×)
  4. washThe combined EtOAc layers were washed (brine)
  5. dry with materialdried (MgSO4)
  6. filtrationfiltered
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-f2db9d22d5154db5a0d3ad6dc5f475cf
출처 데이터셋
uspto-grants-2004_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06743794B2

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