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Dimethylcarbamoyl Chloride → Dimethylcarbamoyloxy-phenyl-acetic acid

HRID 79917
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HRID 79917 반응식
C[O:2][C:3](=[O:12])[CH:4]([OH:11])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.[CH3:13][N:14]([CH3:18])[C:15](Cl)=[O:16]>C1COCC1.CN(C1C=CN=CC=1)C.C(OCC)(=O)C>[CH3:13][N:14]([CH3:18])[C:15]([O:11][CH:4]([C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)[C:3]([OH:2])=[O:12])=[O:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 6598Dimethylcarbamoyl ChlorideHCID 78066(+-)-Methyl mandelate

생성물 1

HCID 66621140Dimethylcarbamoyloxy-phenyl-acetic acid수율 83%

시약·촉매·용매 3

HCID 142844-(Dimethylamino)pyridine촉매HCID 8028Tetrahydrofuran용매HCID 8857Ethyl Acetate
용매

실험 절차

To hydroxyl-phenyl-acetic acid methyl ester (500 mg) in THF (10 mL) were added dimethylcarbamoyl chloride (304 μl), TEA (503 μl), and DMAP (37 mg). After stirring for overnight at room temperature, the mixture was taken up in ethyl acetate (150 mL). The organic phase was washed with 1 N HCl (1×100 mL) and saturated sodium bicarbonate (1×100 mL), and dried over sodium sulfate. After the solvent was removed, the resulting solid was dissolved in THF (6 mL). To the solution was added 2 M LiOH (3 mL). After stirring for 90 min. at room temperature, the reaction mixture was acidified with 2 N HCl (3.2 mL). The mixture was extracted with ethyl acetate (50 mL). The organic phase was dried over sodium sulfate. The solvent was removed under reduced pressure to provide dimethylcarbamoyloxy-phenyl-acetic acid (561 mg, 83%) as an off-white solid.

후처리

  1. washThe organic phase was washed with 1 N HCl (1×100 mL) and saturated sodium bicarbonate (1×100 mL)
  2. dry with materialdried over sodium sulfate
  3. customAfter the solvent was removed
  4. dissolutionthe resulting solid was dissolved in THF (6 mL)
  5. additionTo the solution was added 2 M LiOH (3 mL)
  6. stirringAfter stirring for 90 min. at room temperature
  7. extractionThe mixture was extracted with ethyl acetate (50 mL)
  8. dry with materialThe organic phase was dried over sodium sulfate
  9. customThe solvent was removed under reduced pressure

출처 및 근거

ORD 기록
ord-813a3c31ab4841459d205e36fa83b866
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08841278B2

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