Triethyl phosphonoacetate → ethyl-E-4-(3-methoxyphenyl)-4-methylpent-2-enoate

HRID 1869448노트

반응식

HRID 1869448 반응식
[CH3:1][CH2:2][O:3][C:4]([CH2:6]P(OCC)(OCC)=O)=[O:5].[Li+].CC([N-]C(C)C)C.[CH3:23][O:24][C:25]1[CH:26]=[C:27]([C:31]([CH3:35])([CH3:34])[CH:32]=O)[CH:28]=[CH:29][CH:30]=1.[Cl-].[NH4+]>C1COCC1.CCCCCCC.C(C1C=CC=CC=1)C.O1CCCC1>[CH2:2]([O:3][C:4](=[O:5])/[CH:6]=[CH:35]/[C:31]([C:27]1[CH:28]=[CH:29][CH:30]=[C:25]([O:24][CH3:23])[CH:26]=1)([CH3:32])[CH3:34])[CH3:1]

참가 물질

7

실험 절차

33.6 g (114.3 mmol) of phosphonoacetic acid triethyl ester is introduced into 148 ml of tetrahydrofuran. At 0° C., 79.7 ml of a 2 M solution of LDA in THF/heptane/ethylbenzene is added in drops (1½ hours). After one hour of stirring, 24.3 g (136.34 mmol) of 2-(3-methoxyphenyl)-2-methylpropanal, dissolved in 130 ml of tetrahydrofuran, is added in drops at 0° C. After five days of stirring at room temperature, the reaction mixture is poured into 250 ml of dilute ammonium chloride solution and extracted twice with 400 ml each of diethyl ether. The combined organic extracts are treated as usual, and the residue that is obtained is chromatographed on silica gel (mobile solvent ethyl acetate/hexane). 27.2 g (80.4%) of the desired compound is isolated.

후처리

  1. additionis added in drops at 0° C
  2. stirringAfter five days of stirring at room temperature
  3. extractionextracted twice with 400 ml each of diethyl ether
  4. additionThe combined organic extracts are treated as usual, and the residue that
  5. customis obtained
  6. customis chromatographed on silica gel (mobile solvent ethyl acetate/hexane)

출처 및 근거

ORD 기록
ord-a6c56cfdff1a452ab8f8c13c4eed5ba2
출처 데이터셋
uspto-grants-2009_12
특허 번호
US07638515B2

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