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Ammonia → 1-(3,4-Dimethylphenyl)ethan-1-amine

HRID 660050
ノート
印刷プレビュー

反応式

HRID 660050 の反応式
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([CH3:10])=O)=[CH:4][C:3]=1[CH3:11].[NH3:12].[BH4-].[Na+]>CCCO.CCCO.CCCO.CCCO.[Ti].C(OCC)(=O)C.CO>[CH3:11][C:3]1[CH:4]=[C:5]([CH:8]([NH2:12])[CH3:10])[CH:6]=[CH:7][C:2]=1[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

6

反応物 3

HCID 222Ammonia2 回HCID 771933,4-DimethylacetophenoneHCID 4311764Sodium borohydride

生成物 1

HCID 50864681-(3,4-Dimethylphenyl)ethan-1-amine収率 18%

試薬・触媒・溶媒 2

HCID 4379755Titanium n-propoxide触媒HCID 21584119Ethylacetate methanol
溶媒

実験手順

16.4 ml (150.0 mmol) of tetrapropyl orthotitanate were added to a solution of 4.46 g (30.0 mmol) of 3,4-dimethylacetophenone in a 2 M ethanolic ammonia solution (75 ml), and the mixture was stirred for 6 hours at RT. 1.7 g (45.0 mmol) of sodium borohydride were then added, and stirring was continued for a further 16 hours at RT. Thereafter, the reaction solution was poured into a saturated aqueous ammonia solution (75 ml). The precipitate that formed was filtered off with suction, and then washing with ethyl acetate was carried out. The aqueous filtrate was concentrated in vacuo, followed by extraction twice with ethyl acetate. The combined ethyl acetate phases were extracted three times with 2 M hydrochloric acid. The combined aqueous phases were adjusted to pH 11 with a 2 M aq. NaOH solution and then extracted three times with ethyl acetate. The combined organic phases were dried over MgSO4, filtered and concentrated in vacuo. CC (ethyl acetate/MeOH 9:1) yielded 799 mg (5.4 mmol, 18%) of 1-(3,4-dimethylphenyl)ethylamine.

後処理

  1. stirringstirring
  2. waitwas continued for a further 16 hours at RT
  3. customThe precipitate that formed
  4. filtrationwas filtered off with suction
  5. washwashing with ethyl acetate
  6. concentrationThe aqueous filtrate was concentrated in vacuo
  7. extractionfollowed by extraction twice with ethyl acetate
  8. extractionThe combined ethyl acetate phases were extracted three times with 2 M hydrochloric acid
  9. extractionextracted three times with ethyl acetate
  10. dry with materialThe combined organic phases were dried over MgSO4
  11. filtrationfiltered
  12. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-ba02396c21e84cc49b866231a613e00b
出典データセット
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08084470B2

反応ノート

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