Ethyl Bromide → 5-(Ethylamino)-2-methylphenol

HRID 2052526ノート

反応式

HRID 2052526 の反応式
[CH2:1](Br)[CH3:2].[NH2:4][C:5]1[CH:6]=[CH:7][C:8]([CH3:12])=[C:9]([OH:11])[CH:10]=1.C(=O)([O-])[O-].[Na+].[Na+]>C(O)C.O>[CH2:1]([NH:4][C:5]1[CH:6]=[CH:7][C:8]([CH3:12])=[C:9]([OH:11])[CH:10]=1)[CH3:2]

参加物

6

実験手順

88.6 gm of ethyl bromide were added to a solution of 50 gm of 5-amino-2-methylphenol in 250 ml of ethanol; and the mixture was refluxed for four hours. After the solution had cooled, it was diluted with 1.2 liters of water and was made weakly alkaline with sodium carbonate. After repeated extraction with ether, the ether extracts were dried and concentrated. The residue was recrystallized from ethanol, and had a melting point of 128° C. to 129° C.

後処理

  1. temperatureand the mixture was refluxed for four hours
  2. temperatureAfter the solution had cooled
  3. extractionextraction with ether
  4. dry with materialthe ether extracts were dried
  5. concentrationconcentrated
  6. customThe residue was recrystallized from ethanol

出典と根拠

ORDレコード
ord-f30ad37330bc41f895fe9d47caa7b121
出典データセット
uspto-grants-1980_01
特許番号
USRE030199

反応ノート

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