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Hydrochloric Acid → 3-(Benzyloxy)-6-bromo-4-methoxypicolinic acid

HRID 1059659
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HRID 1059659 반응식
Br[C:2]1[CH:7]=[C:6]([Br:8])[N:5]=[C:4]([C:9]([O:11]C)=[O:10])[C:3]=1[O:13][CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.[C:21](=O)([O-])[O-:22].[K+].[K+].CO.Cl>O>[Br:8][C:6]1[N:5]=[C:4]([C:9]([OH:11])=[O:10])[C:3]([O:13][CH2:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)=[C:2]([O:22][CH3:21])[CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 887MethanolHCID 11430Potassium CarbonateHCID 22175074Methyl 3-(benzyloxy)-4,6-dibromopicolinate

생성물 1

HCID 221750843-(Benzyloxy)-6-bromo-4-methoxypicolinic acid수율 95.3%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A vigorously stirred mixture of 15 (25.5 g), potassium carbonate (75 g) and methanol (300 mL) was heated at reflux for 30 hours. The mixture was cooled, poured into water (800 mL), and the pH adjusted to 2 by the addition of conc. HCl. The resulting mixture was extracted with CH2Cl2 (3×150 mL). The organic extracts were combined, dried (MgSO4) and the solvent was evaporated to give a nearly colorless oil (20.5 g) which slowly solidified upon standing. This was recrystallized from methanol (125 mL)/water (40 mL) to give the desired acid 16 (11.6 g), m.p. 134-135° C.

후처리

  1. temperaturewas heated
  2. temperatureat reflux for 30 hours
  3. temperatureThe mixture was cooled
  4. extractionThe resulting mixture was extracted with CH2Cl2 (3×150 mL)
  5. dry with materialdried (MgSO4)
  6. customthe solvent was evaporated

출처 및 근거

ORD 기록
ord-d714a4837050406ab6c8121687c73e98
출처 데이터셋
uspto-grants-2003_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06521622B1

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