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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Lithium hydroxide, monohydrate → 5-(2,2,2-Trifluoroethoxy)pyridine-2-carboxylic acid

HRID 405731
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HRID 405731 반응식
C[O:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([O:11][CH2:12][C:13]([F:16])([F:15])[F:14])=[CH:7][N:6]=1)=[O:4].O.[OH-].[Li+]>CO>[F:16][C:13]([F:14])([F:15])[CH2:12][O:11][C:8]1[CH:9]=[CH:10][C:5]([C:3]([OH:4])=[O:2])=[N:6][CH:7]=1
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참가 물질

4

반응물 2

HCID 168937Lithium hydroxide, monohydrateHCID 57475873Methyl 5-(2,2,2-trifluoroethoxy)pyridine-2-carboxylate

생성물 1

HCID 574758545-(2,2,2-Trifluoroethoxy)pyridine-2-carboxylic acid

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

Under an atmosphere of nitrogen a solution of 5-(2,2,2-trifluoro-ethoxy)-pyridine-2-carboxylic acid methyl ester (216 mg, 0.92 mmol) in methanol (1 ml) was treated with a solution of lithium hydroxide monohydrate (78 mg, 1.84 mmol) in methanol (0.1 ml). After stirring for 2 hours the reaction mixture was evaporated at reduced pressure. The residue was treated with hydrochloric acid (1N), the solid material was filtered then washed with water, finally dried at high vacuum. The 5-(2,2,2-trifluoro-ethoxy)-pyridine-2-carboxylic acid was obtained as a white solid (125 mg, 61% of theory).

후처리

  1. customwas evaporated at reduced pressure
  2. additionThe residue was treated with hydrochloric acid (1N)
  3. filtrationthe solid material was filtered
  4. washthen washed with water
  5. customfinally dried at high vacuum

출처 및 근거

ORD 기록
ord-a2a73a5c8fca492a931b986271e91a6c
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08754075B2

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