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Sodium Methoxide → 5-(3,4-Dimethoxyphenyl)-4,5-dihydro-1,3-oxazol-2-ol

HRID 2052558
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인쇄 미리보기

반응식

HRID 2052558 반응식
C([O:3][C:4](=[O:19])[NH:5][CH2:6][CH:7]([C:9]1[CH:14]=[CH:13][C:12]([O:15][CH3:16])=[C:11]([O:17][CH3:18])[CH:10]=1)O)C.C[O-].[Na+]>C1(C)C=CC=CC=1>[CH3:18][O:17][C:11]1[CH:10]=[C:9]([CH:7]2[O:19][C:4](=[O:3])[NH:5][CH2:6]2)[CH:14]=[CH:13][C:12]=1[O:15][CH3:16]
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참가 물질

4

반응물 2

HCID 10942334Sodium MethoxideHCID 53831097Ethyl (2-(3,4-dimethoxyphenyl)-2-hydroxyethyl)carbamate

생성물 1

HCID 30506615-(3,4-Dimethoxyphenyl)-4,5-dihydro-1,3-oxazol-2-ol수율 80%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

3 mmol of 2-(3,4-dimethoxyphenyl)-2-hydroxyethylcarbamic acid ethyl ester is suspended with 4 mmol of sodium methylate in 12 ml. of toluene and heated for 2 hours to a bath temperature of 110° under the exclusion of moisture. During this step, methanol and ethanol are distilled off. The toluene is then withdrawn under vacuum, the residue is taken up in 50 ml. of chloroform and distributed over 10 ml. of water. After drying, filtration, and concentration of the organic phase, the mixture is recrystallized from methanol, thus obtaining an 80% yield of 5-(3,4-dimethoxyphenyl)-2-oxazolidinone, m.p. 114°-117°.

후처리

  1. distillationDuring this step, methanol and ethanol are distilled off
  2. customThe toluene is then withdrawn under vacuum
  3. customAfter drying
  4. filtrationfiltration, and concentration of the organic phase
  5. customthe mixture is recrystallized from methanol

출처 및 근거

ORD 기록
ord-a45e7795cf214c579e9bf74e8394bc09
출처 데이터셋
uspto-grants-1980_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04186129

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