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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Citric Acid → 4-((Tert-butoxy)carbonyl)morpholine-2-carboxylic acid

HRID 602132
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인쇄 미리보기

반응식

HRID 602132 반응식
[OH-].[K+].[C:3]([O:7][C:8]([N:10]1[CH2:15][CH2:14][O:13][CH:12]([C:16]([O:18]C)=[O:17])[CH2:11]1)=[O:9])([CH3:6])([CH3:5])[CH3:4].O.C(O)(=O)CC(CC(O)=O)(C(O)=O)O>CO>[C:3]([O:7][C:8]([N:10]1[CH2:15][CH2:14][O:13][CH:12]([C:16]([OH:18])=[O:17])[CH2:11]1)=[O:9])([CH3:6])([CH3:4])[CH3:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 311Citric AcidHCID 962WaterHCID 14797Potassium HydroxideHCID 588174744-tert-Butyl 2-methyl morpholine-2,4-dicarboxylate

생성물 1

HCID 27559654-((Tert-butoxy)carbonyl)morpholine-2-carboxylic acid수율 93%

시약·촉매·용매 1

HCID 887Methanol
용매

실험 절차

A 1 mol/L aqueous potassium hydroxide solution (3 mL) was added to methyl 4-(tert-butoxycarbonyl)morpholine-2-carboxylate (251 mg, 1.02 mmol) in methanol (15 mL). The mixture was stirred at room temperature for 8 hours. Subsequently, water was added to the mixture, followed by addition of a 5% aqueous citric acid solution to make the mixture acidic. The mixture was then extracted with ethyl acetate. The extract was washed with brine and was dried over magnesium sulfate. Evaporation of the solvent gave 219 mg (93%) of the desired compound as a colorless powder.

후처리

  1. extractionThe mixture was then extracted with ethyl acetate
  2. washThe extract was washed with brine
  3. dry with materialwas dried over magnesium sulfate
  4. customEvaporation of the solvent

출처 및 근거

ORD 기록
ord-52c0185b802d4cea9b27386c3abe2c19
출처 데이터셋
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07902367B2

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