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Hydrochloric Acid → 2-Benzyloxy-5-(2-hydroxyethyl)benzamide

HRID 1862621
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HRID 1862621 반응식
[CH2:1]([O:8][C:9]1[CH:17]=[CH:16][C:15]([CH2:18][CH2:19][O:20]COC)=[CH:14][C:10]=1[C:11]([NH2:13])=[O:12])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl.O>CO>[CH2:1]([O:8][C:9]1[CH:17]=[CH:16][C:15]([CH2:18][CH2:19][OH:20])=[CH:14][C:10]=1[C:11]([NH2:13])=[O:12])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 962WaterHCID 186201822-Benzyloxy-5-(2-methoxymethoxyethyl)benzamide

생성물 1

HCID 186200672-Benzyloxy-5-(2-hydroxyethyl)benzamide수율 83.7%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of 2-benzyloxy-5-(2-methoxymethoxyethyl)benzamide (721 mg) in methanol (10 ml) was added concentrated hydrochloric acid (0.7 ml), and the mixture was heated under reflux for 1 hour with stirring. Water was added to the reaction mixture, and the resulting mixture was extracted with ethyl acetate. The extract was washed with brine and dried over anhydrous magnesium sulfate. After the solvent was removed under reduced pressure, diethyl ether was added to the residue, and the resulting insoluble material was collected by filtration to give 2-benzyloxy-5-(2-hydroxyethyl)benzamide (519 mg).

후처리

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 1 hour
  3. extractionthe resulting mixture was extracted with ethyl acetate
  4. washThe extract was washed with brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customAfter the solvent was removed under reduced pressure, diethyl ether
  7. additionwas added to the residue
  8. filtrationthe resulting insoluble material was collected by filtration

출처 및 근거

ORD 기록
ord-2ae88990561d415f98aaa082d9a66f12
출처 데이터셋
uspto-grants-2003_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06538152B1

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