Phosphorus tribromide → 3-Bromo-5-(bromomethyl)-2-(2,4-difluorophenoxy)pyridine

HRID 633556ノート

反応式

HRID 633556 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([CH2:17]O)[CH:5]=[N:6][C:7]=1[O:8][C:9]1[CH:14]=[CH:13][C:12]([F:15])=[CH:11][C:10]=1[F:16].[Br:19]P(Br)Br.C(=O)(O)[O-].[Na+]>ClCCl>[Br:1][C:2]1[C:7]([O:8][C:9]2[CH:14]=[CH:13][C:12]([F:15])=[CH:11][C:10]=2[F:16])=[N:6][CH:5]=[C:4]([CH2:17][Br:19])[CH:3]=1

参加物

5

反応物 3

HCID 24614Phosphorus tribromideHCID 516892Sodium BicarbonateHCID 86721075(5-Bromo-6-(2,4-difluorophenoxy)pyridin-3-yl)methanol

生成物 1

HCID 867210763-Bromo-5-(bromomethyl)-2-(2,4-difluorophenoxy)pyridine収率 86%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

A solution of the product from Example 60B (0.73 g, 2.309 mmol) in dichloromethane (11.55 mL) under nitrogen was treated dropwise with tribromophosphine (0.218 mL, 2.309 mmol), stirred for one hour and poured into ice water and the pH was adjusted to pH 9 by addition of solid sodium bicarbonate added portionwise. An emulsion formed that was partially removed by filtration. The aqueous layer was extracted with dichloromethane and the organics were combined, washed with saturated aqueous sodium chloride, dried (anhydrous Na2SO4) filtered, and concentrated to afford the title compound (0.75 g, 86%).

後処理

  1. additionadded portionwise
  2. customAn emulsion formed
  3. customthat was partially removed by filtration
  4. extractionThe aqueous layer was extracted with dichloromethane
  5. washwashed with saturated aqueous sodium chloride
  6. dry with materialdried (anhydrous Na2SO4)
  7. filtrationfiltered
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-123677e76dc94c9ea82b3a31ec37ba76
出典データセット
uspto-grants-2016_04
特許番号
US09321764B2

反応ノート

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