4-Bromopyridine-3-carbaldehyde → 1-(4-Bromo-pyridin-3-yl)-2-methyl-propan-1-ol

HRID 1712072

反応式

HRID 1712072 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][N:5]=[CH:4][C:3]=1[CH:8]=[O:9].[CH:10]([Mg]Br)([CH3:12])[CH3:11]>C1COCC1>[Br:1][C:2]1[CH:7]=[CH:6][N:5]=[CH:4][C:3]=1[CH:8]([OH:9])[CH:10]([CH3:12])[CH3:11]

参加物

4

反応物 2

HCID 111167404-Bromopyridine-3-carbaldehydeHCID 178418365HCID 178418365、化合物

生成物 1

HCID 592051921-(4-Bromo-pyridin-3-yl)-2-methyl-propan-1-ol

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

To a solution of 4-bromo-pyridine-3-carbaldehyde (400 mg, 2.15 mmol) in THF (10 mL) at −78° C. was added dropwise 1.0 M isopropyl-magnesium bromide solution in THF (3.23 mL). After 15 min, the reaction was quenched with saturated ammonium chloride solution and extracted with ethyl acetate, then purification by flash chromatography eluted with 50% ethyl acetate in hexane to yield 1-(4-bromo-pyridin-3-yl)-2-methyl-propan-1-ol as slight yellow crystals.

後処理

  1. customthe reaction was quenched with saturated ammonium chloride solution
  2. extractionextracted with ethyl acetate
  3. custompurification by flash chromatography
  4. washeluted with 50% ethyl acetate in hexane

出典と根拠

ORDレコード
ord-db9281c220384cdb9385a95dea3da23b
出典データセット
uspto-grants-2010_09
特許番号
US07790895B2

関連ノート

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