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Potassium Carbonate → Methyl 4-(6-methoxypyridin-3-yl)-3,5-dimethylbenzoate

HRID 531246
ノート
印刷プレビュー

反応式

HRID 531246 の反応式
[CH3:1][C:2]1[CH:3]=[C:4]([CH:9]=[C:10]([CH3:21])[C:11]=1B1OC(C)(C)C(C)(C)O1)[C:5]([O:7][CH3:8])=[O:6].Br[C:23]1[CH:24]=[CH:25][C:26]([O:29][CH3:30])=[N:27][CH:28]=1.C(=O)([O-])[O-].[K+].[K+]>[Pd](Cl)Cl.C(P(C(C)(C)C)[C-]1C=CC=C1)(C)(C)C.[C-]1(P(C(C)(C)C)C(C)(C)C)C=CC=C1.[Fe+2].O1CCOCC1>[CH3:30][O:29][C:26]1[N:27]=[CH:28][C:23]([C:11]2[C:10]([CH3:21])=[CH:9][C:4]([C:5]([O:7][CH3:8])=[O:6])=[CH:3][C:2]=2[CH3:1])=[CH:24][CH:25]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 11430Potassium CarbonateHCID 27348955-Bromo-2-methoxypyridineHCID 68021937Methyl 3,5-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate

生成物 1

HCID 90009124Methyl 4-(6-methoxypyridin-3-yl)-3,5-dimethylbenzoate

試薬・触媒・溶媒 2

HCID 178454861HCID 178454861、化合物触媒
HCID 31275
1,4-Dioxane
溶媒

反応条件

温度
80 °C

実験手順

Methyl 3,5-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate (Step A, 2.79 g, 7.20 mmol), 1,1′-bis(di-tert-butylphoshino)ferrocene palladium dichloride (0.391 g, 0.600 mmol) and 5-bromo-2-methoxypyridine (0.776 mL, 6 mmol) were mixed in a reaction flask which was then evacuated and charged with nitrogen three times. Added 1,4-dioxane (30.0 mL) and 3.0M aqueous potassium carbonate (6.00 mL, 18.00 mmol), evacuated and charged with nitrogen (3×), then stirred overnight at 80° C. The reaction was then partitioned between ethyl acetate and water. After a second water wash, the organic was dried over sodium sulfate, filtered and evaporated. The crude was purified by silica gel chromatography, eluting with 10 column volumes of 4% ethyl acetate/hexanes followed by a gradient of 4-10% ethyl acetate/hexanes over 10 column volumes to give the title compound. 1H NMR (CDCl3, 500 MHz) δ7.94 (d, 1H), 67.79 (s, 2H), 67.36 (dd, 1H), 66.84 (d, 1H), 64.00 (s, 3H), 63.93 (s, 3H), 62.09 (s, 6H).

後処理

  1. customwas then evacuated
  2. additioncharged with nitrogen three times
  3. additioncharged with nitrogen (3×)
  4. customThe reaction was then partitioned between ethyl acetate and water
  5. washAfter a second water wash
  6. dry with materialthe organic was dried over sodium sulfate
  7. filtrationfiltered
  8. customevaporated
  9. customThe crude was purified by silica gel chromatography
  10. washeluting with 10 column volumes of 4% ethyl acetate/hexanes

出典と根拠

ORDレコード
ord-6a33b7209045487d9cb1d3b95263d935
出典データセット
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09353101B2

反応ノート

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