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Sodium potassium tartrate tetrahydrate → HCID 71606902, 화합물

HRID 623946
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HRID 623946 반응식
[Br:1][C:2]1[CH:3]=[C:4]([O:12]C)[C:5]([C:8]([F:11])([F:10])[F:9])=[N:6][CH:7]=1.O.O.O.O.C(C(C(C([O-])=O)O)O)([O-])=O.[Na+].[K+]>C(O)(=O)C.Br.C(OCC)(=O)C>[Br:1][C:2]1[CH:3]=[C:4]([OH:12])[C:5]([C:8]([F:9])([F:10])[F:11])=[N:6][CH:7]=1
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참가 물질

6

반응물 2

HCID 2724148Sodium potassium tartrate tetrahydrateHCID 576341775-Bromo-3-methoxy-2-(trifluoromethyl)pyridine

생성물 1

HCID 71606902HCID 71606902, 화합물수율 79%

시약·촉매·용매 3

HCID 176Acetic Acid용매2회HCID 260Hydrogen Bromide용매HCID 8857
Ethyl Acetate
용매

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온도
110 °C

실험 절차

A solution of 5-bromo-3-methoxy-2-(trifluoromethyl)pyridine (28) (0.87 g, 3.4 mmol) in a mixture of acetic acid (6 mL) and 33% HBr in acetic acid (12 mL) was stirred at 110° C. in a sealed tube overnight. Then Potassium Sodium tartrate tetrahydrate (7.8 g) was added slowly under 0° C. The mixture was taken up in ethyl acetate after 10 minutes stirring, the organic phase was washed with brine, dried over Na2SO4. The extract was concentrated under reduced pressure. The residue was purified by column chromatography on silica gel using a gradient of Hexane-Ethyl acetate (1:2) as the eluent to give the product (29) 0.65 g as gray solid, Yield: 79%. 1H NMR (CD3OD, 400 MHz): δ 8.18 (s, 1H), 7.58 (s, 1H). 19F NMR (CDCl3, 376 MHz): −68.0.

후처리

  1. stirringstirring
  2. washthe organic phase was washed with brine
  3. dry with materialdried over Na2SO4
  4. concentrationThe extract was concentrated under reduced pressure
  5. customThe residue was purified by column chromatography on silica gel using a gradient of Hexane-Ethyl acetate (1:2) as the eluent

출처 및 근거

ORD 기록
ord-356d1c9596b64bff829f5f2057c3747f
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09303017B2

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