Hydrochloric Acid → 4-[2-(Diethylamino)ethyl]aniline

HRID 641062

反応式

HRID 641062 の反応式
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([N:11]([CH2:14][CH3:15])[CH2:12][CH3:13])=O)=[CH:4][CH:3]=1.NC1C=CC(CC(N)=O)=CC=1.CSC.B.Cl.[OH-].[Na+]>C1COCC1>[CH2:14]([N:11]([CH2:12][CH3:13])[CH2:9][CH2:8][C:5]1[CH:4]=[CH:3][C:2]([NH2:1])=[CH:7][CH:6]=1)[CH3:15]

参加物

7

反応物 5

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 2380342-(4-Aminophenyl)acetamideHCID 12423031(Dimethyl sulfide)trihydroboronHCID 16775389HCID 16775389、化合物

生成物 1

HCID 225692664-[2-(Diethylamino)ethyl]aniline収率 86%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

To a solution of 2-(4-aminophenyl)-N,N-diethylacetamide, (2-NB-2-A13; 1.5 g, 7.28 mmol) from Step 2 in anhydrous THF (15 mL) kept at 0° C. was added a 2 M solution of borane dimethylsulfide in THF (14.5 mL, 29 mmol) slowly. The reaction was allowed to warm to room temperature and stirred for 18 h. Hydrochloric acid (6N, 10 mL) was carefully added and the reaction was refluxed for 1 hour followed by cooling to room temperature and neutralization with 3N sodium hydroxide solution. Aqueous layer was separated and extracted with ethyl acetate (4×30 mL). Combined organic layer was dried over sodium sulfate, filtered and evaporated to provide 4-(2-(diethylamino)ethyl)aniline as a light-brown oil (1.25 g, 86%).

後処理

  1. customkept at 0° C.
  2. temperaturethe reaction was refluxed for 1 hour
  3. temperatureby cooling to room temperature
  4. customAqueous layer was separated
  5. extractionextracted with ethyl acetate (4×30 mL)
  6. dry with materialCombined organic layer was dried over sodium sulfate
  7. filtrationfiltered
  8. customevaporated

出典と根拠

ORDレコード
ord-9f939849868e4113b94cf81b2d00c8cc
出典データセット
uspto-grants-2010_04
特許番号
US07692005B2

関連ノート

読み込み中…