2-Methyl-2-butanol → HCID 178526251、化合物

HRID 497547

反応式

HRID 497547 の反応式
Cl[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N+:3]=1[O-:8].[NH2:9][CH2:10][CH2:11][CH2:12][OH:13].C([O-])(O)=O.[Na+].C(O)(CC)(C)C>C(Cl)Cl>[OH:13][CH2:12][CH2:11][CH2:10][NH:9][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N+:3]=1[O-:8]

参加物

6

反応条件

温度
67 °C

実験手順

A mixture of 2-chloropyridine-N-oxide (16.6 g, 100 mmoles), 3-amino-1-propanol (15.3 ml, 200 mmoles), NaHCO3 (42 g, 0.5 mole), and tert-amyl alcohol (100 ml) was heated to reflux. After 23 hours, the reaction was cooled, diluted with CH2Cl2 (300 ml), and filtered to remove insoluble materials. The filtrate was concentrated to afford a brown oil. The oil was dried under vacuum overnight. Ether (100 ml) was added to give a brown solid. The ether was decanted and the solid was washed further with ether/acetonitrile (3/1). The resulting solid was heated at 67° C. under vacuum to give the desired product (13.5 g). 1H NMR was consistent with the proposed structure.

後処理

  1. temperaturewas heated to reflux
  2. temperaturethe reaction was cooled
  3. filtrationfiltered
  4. customto remove insoluble materials
  5. concentrationThe filtrate was concentrated
  6. customto afford a brown oil
  7. customThe oil was dried under vacuum overnight
  8. additionEther (100 ml) was added
  9. customto give a brown solid
  10. customThe ether was decanted
  11. washthe solid was washed further with ether/acetonitrile (3/1)

出典と根拠

ORDレコード
ord-7638cfb683b8452eb81dd8e69519514f
出典データセット
uspto-grants-2005_09
特許番号
US06949578B2

関連ノート

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