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Potassium Hydroxide → 2-[(4-Fluorophenethyl)oxy]ethylamine

HRID 1422278
ノート
印刷プレビュー

反応式

HRID 1422278 の反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][O:10][CH2:11][CH2:12][NH:13]C(=O)OC)=[CH:4][CH:3]=1.[OH-].[K+].O.NN>C(O)CO.O>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][CH2:9][O:10][CH2:11][CH2:12][NH2:13])=[CH:6][CH:7]=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 14797Potassium HydroxideHCID 24654Hydrazine hydrate (1:1)HCID 18779044Methyl N-[2-(2-(4-fluorophenyl)ethoxy)ethyl]carbamate

生成物 1

HCID 187790642-[(4-Fluorophenethyl)oxy]ethylamine

試薬・触媒・溶媒 2

HCID 174Ethylene Glycol溶媒HCID 962Water溶媒

実験手順

The product of step d) (8.0 g) was dissolved in ethylene glycol and to this was added potassium hydroxide (48 g) and hydrazine hydrate (8.3 ml). The stirred mixture was heated to 140° for 4 hours then allowed to cool to room temperature overnight. The mixture was then diluted with water and extracted with diethyl ether (x3). The combined organic extracts were washed with brine, dried (MgOS4) and filtered. The volatiles were removed in vacuo to give the subtitle compound (5.36 g).

後処理

  1. temperatureThe stirred mixture was heated to 140° for 4 hours
  2. extractionextracted with diethyl ether (x3)
  3. washThe combined organic extracts were washed with brine
  4. dry with materialdried (MgOS4)
  5. filtrationfiltered
  6. customThe volatiles were removed in vacuo

出典と根拠

ORDレコード
ord-b941b40684994b01b2149ef4bbb1fc88
出典データセット
uspto-grants-2000_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06080869

反応ノート

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