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Sodium hydride → (R)-2((1-(Benzyloxy)propan-2-yl)oxy)-3-bromopyridine

HRID 1524089
ノート
印刷プレビュー

反応式

HRID 1524089 の反応式
[CH2:1]([O:8][CH2:9][C@H:10]([OH:12])[CH3:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H-].[Na+].[Br:15][C:16]1[C:17](Cl)=[N:18][CH:19]=[CH:20][CH:21]=1>CN(C=O)C>[CH2:1]([O:8][CH2:9][C@H:10]([O:12][C:17]1[C:16]([Br:15])=[CH:21][CH:20]=[CH:19][N:18]=1)[CH3:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 24758Sodium hydrideHCID 6933243-Bromo-2-chloropyridineHCID 10953891(2R)-1-(benzyloxy)propan-2-ol

生成物 1

HCID 90313507(R)-2((1-(Benzyloxy)propan-2-yl)oxy)-3-bromopyridine

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

To a stirred solution of (R)-1-(benzyloxy)propan-2-ol (2.0 g, 12 mmol) in dry DMF (5 mL) was added NaH (1.5 g, 36 mmol) at 0 Celsius. The reaction mixture was then stirred for 30 min before adding 3-bromo-2-chloropyridine (2.3 g, 12 mmol) and stirring continued for another 4 h. The reaction was quenched by slow addition of water (10 mL) and the resultant mixture extracted with ethyl acetate (3×10 mL). The combined organic extracts were dried over Na2SO4, filtered, concentrated to dryness, and the crude product purified by FCC to provide the title compound.

後処理

  1. stirringstirring
  2. waitcontinued for another 4 h
  3. customThe reaction was quenched by slow addition of water (10 mL)
  4. extractionthe resultant mixture extracted with ethyl acetate (3×10 mL)
  5. dry with materialThe combined organic extracts were dried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated to dryness
  8. customthe crude product purified by FCC

出典と根拠

ORDレコード
ord-a7a9d52943af488786797a4057051757
出典データセット
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09079866B2

反応ノート

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