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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Sodium Hydroxide → [(3,4,4-Trifluoro-3-butenyl)amino]oxoacetic acid

HRID 54740
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HRID 54740 반응식
O=[C:2]([NH:9][C:10](=[O:15])[C:11]([O:13]C)=[O:12])[CH2:3][C:4]([F:8])=[C:5]([F:7])[F:6].[OH-].[Na+]>CO.O>[F:8][C:4](=[C:5]([F:6])[F:7])[CH2:3][CH2:2][NH:9][C:10](=[O:15])[C:11]([OH:13])=[O:12]
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참가 물질

5

반응물 2

HCID 14798Sodium HydroxideHCID 86748464Oxo[(3,4,4-trifluoro-3-butenyl)amino]oxoacetic acid, methyl ester

생성물 1

HCID 15239198[(3,4,4-Trifluoro-3-butenyl)amino]oxoacetic acid수율 25.4%

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매

실험 절차

A solution of Compound 142 (3.16 g, 0.015 mole) in methanol (25 mL) is treated with a solution of NaOH (0.8 g, 0.02 mole) in water (5 mL). The solution is stirred at room temperature for 30 min and concentrated. The residue is dissolved in water (20 mL) and extracted with dichloromethane (2×30 mL). The aqueous layer is acidified with conc. HCl and extracted with ethyl acetate. The organic layer is dried and evaporated to give 0.75 g of the title compound as a white solid, a 25% yield. m.p. 95°-100° C.

후처리

  1. concentrationconcentrated
  2. dissolutionThe residue is dissolved in water (20 mL)
  3. extractionextracted with dichloromethane (2×30 mL)
  4. extractionextracted with ethyl acetate
  5. customThe organic layer is dried
  6. customevaporated

출처 및 근거

ORD 기록
ord-1e65195886854ef28b1d1bbb05279448
출처 데이터셋
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05623084

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