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Methanol → Methyl 4-amino-6-chloro-5-fluoropicolinate

HRID 407224
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HRID 407224 반응식
[NH2:1][C:2]1[C:7]([F:8])=[C:6]([Cl:9])[N:5]=[C:4]([C:10]([OH:12])=[O:11])[CH:3]=1.S(Cl)(Cl)=O.[CH3:17]O>O>[NH2:1][C:2]1[C:7]([F:8])=[C:6]([Cl:9])[N:5]=[C:4]([C:10]([O:12][CH3:17])=[O:11])[CH:3]=1
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참가 물질

5

반응물 3

HCID 887MethanolHCID 24386Thionyl ChlorideHCID 866754064-Amino-6-chloro-5-fluoropicolinic acid

생성물 1

HCID 86668302Methyl 4-amino-6-chloro-5-fluoropicolinate수율 86%

시약·촉매·용매 1

HCID 962Water용매

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온도
50 °C

실험 절차

To a solution of 4-amino-6-chloro-5-fluoropicolinic acid (23.8 g, 125 mmol) in MeOH (400 ml), cooled in an ice water bath, thionyl chloride (11.78 ml, 162 mmol) was added. The reaction mixture was heated to an internal temperature of 50° C., for 8 hours. The reaction mixture was then diluted with H2O, and extracted with EtOAC (3×100 mL). The combined organics were washed with Sat. NaCl, dried over Mg Sulfate, filtered and concentrated under vacuum to give methyl 4-amino-6-chloro-5-fluoropicolinate (21.9 g, 107 mmol, 86% yield).

후처리

  1. extractionextracted with EtOAC (3×100 mL)
  2. washThe combined organics were washed with Sat. NaCl
  3. dry with materialdried over Mg Sulfate
  4. filtrationfiltered
  5. concentrationconcentrated under vacuum

출처 및 근거

ORD 기록
ord-900fdc93d6034433a65e442fc56cdd91
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08754229B2

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