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Hydrochloric Acid → 5-Bromo-6-cyanopicolinic acid

HRID 474198
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HRID 474198 반응식
C[O:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([Br:11])=[C:7]([C:12]#[N:13])[N:6]=1)=[O:4].Cl>C1COCC1>[Br:11][C:8]1[CH:9]=[CH:10][C:5]([C:3]([OH:4])=[O:2])=[N:6][C:7]=1[C:12]#[N:13]
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참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 57356968Methyl 5-bromo-6-cyanopicolinate

생성물 1

HCID 574252995-Bromo-6-cyanopicolinic acid수율 105.4%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
50 °C

실험 절차

To a solution of potassium trimethylsilanoate (0.80 g, 6.22 mmol) in THF (26 mL) was added 5-bromo-6-cyano-pyridine-2-carboxylic acid methyl ester (998 mg, 4.15 mmol). The mixture was heated at 50° C. for 3 h, then was cooled to rt and treated with HCl (4 N in dioxane; 1.60 mL). After 30 min, the mixture was concentrated. The residue was dissolved in hot EtOAc and filtered. The filtrate was concentrated to give the title compound (993 mg, >100%), which was used in the next step without further purification.

후처리

  1. temperaturewas cooled to rt
  2. concentrationthe mixture was concentrated
  3. dissolutionThe residue was dissolved in hot EtOAc
  4. filtrationfiltered
  5. concentrationThe filtrate was concentrated

출처 및 근거

ORD 기록
ord-91c71256c99440658fb70c75f9f02a8f
출처 데이터셋
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08637520B2

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