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Benzene → HCID 66811298, 화합물

HRID 1097407
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HRID 1097407 반응식
[H-].[Na+].CCOP([O:11][C:12]([CH3:14])=[O:13])(OCC)=O.[CH:15]1[C:20]2[CH2:21][CH2:22][CH2:23][CH2:24][CH:25]([CH2:26][CH:27]=O)[C:19]=2[CH:18]=[CH:17][CH:16]=1.[Cl-].[NH4+].[CH:31]1C=CC=C[CH:32]=1>>[CH:15]1[C:20]2[CH2:21][CH2:22][CH2:23][CH2:24][CH:25]([CH2:26][CH:27]=[CH:14][C:12]([O:11][CH2:31][CH3:32])=[O:13])[C:19]=2[CH:18]=[CH:17][CH:16]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 5

HCID 241Benzene2회HCID 18353Acetic acid, anhydride with diethyl hydrogen phosphateHCID 24758Sodium hydrideHCID 25517Ammonium ChlorideHCID 86657329HCID 86657329, 화합물

생성물 1

HCID 66811298HCID 66811298, 화합물수율 94%

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온도
0 °C

실험 절차

A suspension of sodium hydride (60%, 0.130 g) in anhydrous benzene (5 ml) was slowly added with diethyl phosphonoacetate (0.750 g) at 0° C., and the mixture was stirred at 0° C. for 10 minutes. The mixture was added with a solution of (6,7,8,9-tetrahydro-5H-5-benzocycloheptenyl)acetaldehyde (0.419 g) in anhydrous benzene (5 ml), and the mixture was stirred at 0° C. for 5 minutes, and then refluxed overnight by heating. The reaction mixture was left to cool and then added with saturated aqueous ammonium chloride, and the mixture was extracted with ethyl acetate. The organic layer was washed successively with water and saturated brine, and dried over anhydrous sodium sulfate. The organic layer was concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (developing solvent: ethyl acetate:n-hexane=1:300) to obtain the title compound (0.544 g, yield: 94%).

후처리

  1. stirringthe mixture was stirred at 0° C. for 5 minutes
  2. temperaturerefluxed overnight
  3. temperatureby heating
  4. waitThe reaction mixture was left
  5. temperatureto cool
  6. extractionthe mixture was extracted with ethyl acetate
  7. washThe organic layer was washed successively with water and saturated brine
  8. dry with materialdried over anhydrous sodium sulfate
  9. concentrationThe organic layer was concentrated under reduced pressure
  10. customthe resulting residue was purified by silica gel column chromatography (developing solvent: ethyl acetate:n-hexane=1:300)

출처 및 근거

ORD 기록
ord-f0d2cc75700d4154a13c47813711669d
출처 데이터셋
uspto-grants-2012_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08143260B2

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