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Potassium Carbonate → 2-([(Benzyloxy)carbonyl]amino)-3-methoxypropanoic acid

HRID 1882738
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HRID 1882738 반응식
C[O:2][C:3](=[O:19])[CH:4]([NH:8][C:9]([O:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)=[O:10])[CH2:5][O:6][CH3:7].C([O-])([O-])=O.[K+].[K+]>CO>[C:9]([NH:8][CH:4]([CH2:5][O:6][CH3:7])[C:3]([OH:19])=[O:2])([O:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)=[O:10]
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참가 물질

4

반응물 2

HCID 11430Potassium CarbonateHCID 12344754Methyl 2-(((benzyloxy)carbonyl)amino)-3-methoxypropanoate

생성물 1

HCID 123447572-([(Benzyloxy)carbonyl]amino)-3-methoxypropanoic acid수율 95%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

Compound 10 (0.58 g) was dissolved in 80% aqueous methanol (3.0 mL). To this solution was added anhydrous K2CO3 (0.5 g) and the reaction mixture was stirred at room temperature (8 hours). The methanol was evaporated in vacuo and the residue suspended in water (50 mL). The aqueous suspension was washed with ethyl ether (2×25 mL) and then acidified to pH 3.0 using 5N HCl. The acidified aqueous phase was extracted with ethyl acetate (3×25 mL). The ethyl acetate extracts were combined, dried (Na2SO4), filtered, and evaporated in vacuo to obtain pure 11 as a clear viscous oil (0.52 g, 95%): Rf0.30 (10% MeOH/CHCl3).

후처리

  1. customThe methanol was evaporated in vacuo
  2. washThe aqueous suspension was washed with ethyl ether (2×25 mL)
  3. extractionThe acidified aqueous phase was extracted with ethyl acetate (3×25 mL)
  4. dry with materialdried (Na2SO4)
  5. filtrationfiltered
  6. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-50b1fd701d82499f84ab01064d6b0e07
출처 데이터셋
uspto-grants-2004_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
USRE038551E1

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