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Hydrochloric Acid → HCID 54447559、化合物

HRID 975256
ノート
印刷プレビュー

反応式

HRID 975256 の反応式
[CH3:1][O:2][CH2:3][CH2:4][CH2:5][CH2:6]/[C:7](/[C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)=[N:8]/[OH:9].[Br:16][CH2:17][CH2:18]Br.[OH-].[Na+].Cl>[Br-].C([N+](CCCC)(CCCC)CCCC)CCC.ClCCl.O>[Br:16][CH2:17][CH2:18][O:9][N:8]=[C:7]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)[CH2:6][CH2:5][CH2:4][CH2:3][O:2][CH3:1]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 313Hydrochloric AcidHCID 78391,2-DibromoethaneHCID 14798Sodium HydroxideHCID 19971654HCID 19971654、化合物

生成物 1

HCID 54447559HCID 54447559、化合物収率 93.4%

試薬・触媒・溶媒 3

HCID 74236Tetrabutylammonium Bromide触媒
HCID 962
Water
溶媒
HCID 6344Dichloromethane溶媒

実験手順

A mixture of the above oxime (6.5 g, 31 mmol), 1,2-dibromoethane (27 ml, 31 mmol), N,N,N,N-tetrabutylammonium bromide (0.96 g, 3 mmol) and 12N sodium hydroxide (30 ml) was cooled on an icebath with vigorous stirring until the initial exotherm had subsided. The mixture was then stirred at ambient temperature for 16 h. Water (50 ml), 4 N hydrochloric acid (50 ml) and dichloromethane (100 ml) were added and the phases were separated. To the organic phase was added water (50 ml) and pH in the aqueous phase adjusted to 5 with 10% aqueous citric acid. The organic phase was washed with water (50 ml), brine (25 ml) and dried (Na2SO4). The solvent was evaporated in vacuo to give 9.1 g of 5-methoxy-1-phenyl-1-pentanone O-(2-bromoethyl)oxime.

後処理

  1. temperaturewas cooled on an icebath
  2. stirringThe mixture was then stirred at ambient temperature for 16 h
  3. customthe phases were separated
  4. additionTo the organic phase was added water (50 ml)
  5. washThe organic phase was washed with water (50 ml), brine (25 ml)
  6. dry with materialdried (Na2SO4)
  7. customThe solvent was evaporated in vacuo

出典と根拠

ORDレコード
ord-3066d992e0304c888db3e40a576c7fa9
出典データセット
uspto-grants-1997_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05608069

反応ノート

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