Trifluoroacetic acid → N-{4-[2-(4-Methoxyphenyl)ethoxy]benzoyl}glycine

HRID 456267

반응식

HRID 456267 반응식
C(P(=CC#N)(CCCC)CCCC)CCC.C([O:21][C:22](=[O:34])[CH2:23][NH:24][C:25](=[O:33])[C:26]1[CH:31]=[CH:30][C:29]([OH:32])=[CH:28][CH:27]=1)(C)(C)C.[CH3:35][O:36][C:37]1[CH:42]=[CH:41][C:40]([CH2:43][CH2:44]O)=[CH:39][CH:38]=1.FC(F)(F)C(O)=O>ClCCl.O.C1(C)C=CC=CC=1>[CH3:35][O:36][C:37]1[CH:42]=[CH:41][C:40]([CH2:43][CH2:44][O:32][C:29]2[CH:28]=[CH:27][C:26]([C:25]([NH:24][CH2:23][C:22]([OH:21])=[O:34])=[O:33])=[CH:31][CH:30]=2)=[CH:39][CH:38]=1

참가 물질

8

반응물 4

HCID 6422Trifluoroacetic acidHCID 697054-Methoxyphenethyl alcoholHCID 4622928CyanomethylenetributylphosphoraneHCID 10682169N-(4-Hydroxybenzoyl)glycine tert-butyl ester

생성물 1

HCID 66812093N-{4-[2-(4-Methoxyphenyl)ethoxy]benzoyl}glycine수율 72%

시약·촉매·용매 3

HCID 962Water용매HCID 1140Toluene용매HCID 6344Dichloromethane용매

반응 조건

온도
100 °C

실험 절차

(Tributyl phosphoranylidene)acetonitrile (428 μL, 1.50 mmol) was added to a solution of toluene (7 mL) containing N-(4-hydroxybenzoyl)glycine tert-butyl ester (264 mg, 1.05 mmol) prepared in Example 1 (1a) and 2-(4-methoxyphenyl)ethanol (176 mg, 1.16 mmol). The mixture was stirred at 100° C. for 3.5 hours, and then water was added thereto. The mixture was extracted with ethyl acetate. The organic layers were combined, washed with water and saturated brine, and dried over anhydrous magnesium sulfate. Then, the solvent was evaporated. The resulting residue was purified by silica gel column chromatography (hexane to hexane:ethyl acetate, 6:1, 4:1, and 3:1, v/v) to give an oily substance (358 mg). To a solution of dichloromethane (1 mL) containing this oily substance (358 mg, 0.929 mmol), trifluoroacetic acid (0.5 mL) was added. The mixture was stirred at room temperature for 1 hour, and then the solvent was evaporated. Diisopropyl ether was added to the resulting residue to suspend it. The produced precipitate was collected by filtration and was washed with diisopropyl ether to give 248 mg of the title compound (colorless crystalline solid, yield: 72%).

후처리

  1. extractionThe mixture was extracted with ethyl acetate
  2. washwashed with water and saturated brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customThen, the solvent was evaporated
  5. customThe resulting residue was purified by silica gel column chromatography (hexane to hexane
  6. customethyl acetate, 6:1, 4:1, and 3:1, v/v) to give an oily substance (358 mg)
  7. additionwas added
  8. stirringThe mixture was stirred at room temperature for 1 hour
  9. customthe solvent was evaporated
  10. additionDiisopropyl ether was added to the resulting residue
  11. filtrationThe produced precipitate was collected by filtration
  12. washwas washed with diisopropyl ether

출처 및 근거

ORD 기록
ord-96d4e0fadccb4172846f3caba9247330
출처 데이터셋
uspto-grants-2013_07
특허 번호
US08497397B2

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