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Sodium Azide → 11-Amino-1-undecanol

HRID 444615
ノート
印刷プレビュー

反応式

HRID 444615 の反応式
Br[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][OH:13].[N-:14]=[N+]=[N-].[Na+]>C(#N)C.C1COCC1>[NH2:14][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][OH:13]
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 2

HCID 33557Sodium AzideHCID 7416311-Bromo-1-undecanol

生成物 1

HCID 1178995011-Amino-1-undecanol

試薬・触媒・溶媒 2

HCID 6342Acetonitrile溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

11-bromoundecan-1-ol (the compound 31) (15.1 g) was dissolved in 250 ml of acetonitrile, and 15.7 g of sodium azide was added to that, followed by 18-hour reaction caused by refluxing. After cooled down to room temperature, the solid components were removed by filtration. The solvent of the filtrate was distilled away under reduced pressure, to obtain 13.9 g of a transparent, viscous liquid. Of this liquid, 8.34 g was dissolved in 60 ml of THF distilled from calcium hydride in a nitrogen atmosphere, and was cooled in an ice bath. Lithium aluminum hydride (2.53 g) was then dried, and was dissolved in 250 ml of THF. The resultant was dripped, and was then stirred in an ice bath for one hour. After that, 2.5 ml of ion-exchange water, 3.5 ml of 15 wt % aqueous sodium hydride solution, and 7.5 ml of ion-exchange water were added so as to stop reactions. The precipitate generated was removed by filtration, and the solvent of the filtrate was distilled away under reduced pressure. After the filtrate was dried under reduced pressure, the dried filtrate was dissolved in 60 ml of THF, and the same volume of heptane was added to that. The precipitate generated was collected by filtration, to obtain 5.1 g of a white solid 32.

後処理

  1. waitfollowed by 18-hour
  2. customreaction
  3. temperatureby refluxing
  4. customthe solid components were removed by filtration
  5. distillationThe solvent of the filtrate was distilled away under reduced pressure
  6. customto obtain 13.9 g of a transparent, viscous liquid
  7. distillationdistilled from calcium hydride in a nitrogen atmosphere
  8. temperaturewas cooled in an ice bath
  9. dry with materialLithium aluminum hydride (2.53 g) was then dried
  10. dissolutionwas dissolved in 250 ml of THF
  11. additionAfter that, 2.5 ml of ion-exchange water, 3.5 ml of 15 wt % aqueous sodium hydride solution, and 7.5 ml of ion-exchange water were added so as
  12. customThe precipitate generated was removed by filtration
  13. distillationthe solvent of the filtrate was distilled away under reduced pressure
  14. customAfter the filtrate was dried under reduced pressure
  15. dissolutionthe dried filtrate was dissolved in 60 ml of THF
  16. additionthe same volume of heptane was added to that
  17. filtrationThe precipitate generated was collected by filtration

出典と根拠

ORDレコード
ord-7a6ad710c2084428862adfd84858ad82
出典データセット
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08475685B2

反応ノート

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