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

HRID 1059659
ノート
印刷プレビュー

反応式

HRID 1059659 の反応式
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
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-d714a4837050406ab6c8121687c73e98
出典データセット
uspto-grants-2003_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06521622B1

反応ノート

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