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(4-Aminophenoxy)benzene → 6-Phenoxybenzo[d]thiazol-2-amine

HRID 359775
ノート
印刷プレビュー

反応式

HRID 359775 の反応式
[S-:1][C:2]#[N:3].[NH4+].[O:5]([C:12]1[CH:18]=[CH:17][C:15]([NH2:16])=[CH:14][CH:13]=1)[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.BrBr>C(O)(=O)C>[NH2:3][C:2]1[S:1][C:14]2[CH:13]=[C:12]([O:5][C:6]3[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=3)[CH:18]=[CH:17][C:15]=2[N:16]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 8764(4-Aminophenoxy)benzeneHCID 15666Ammonium thiocyanateHCID 24408Bromine

生成物 1

HCID 23449966-Phenoxybenzo[d]thiazol-2-amine収率 65.3%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

反応条件

温度
15 °C

実験手順

20.5 g of ammonium thiocyanate were added to a solution of 25 g of 4-phenoxyaniline in 250 ml of acetic acid, and the mixture was stirred, whilst cooling. While the internal temperature was maintained at 12 to 18° C., 6.95 ml of bromine was added dropwise to the mixture. After completion of the dropwise addition, the mixture was stirred for 2 hours, after which the solvent was removed by evaporation under reduced pressure. 300ml of ethyl acetate and 200 ml of water were added to the residue, and the resulting mixture was neutralized with sodium bicarbonate. The ethyl acetate layer was separated, washed with an aqueous solution of sodium chloride, and then dehydrated over anhydrous magnesium sulfate after which it was concentrated by evaporation under reduced pressure. The solid obtained was triturated in diisopropyl ether, and filtered to give 21.34 g of the title compound, melting at 171-172° C.

後処理

  1. temperaturewhilst cooling
  2. additionAfter completion of the dropwise addition
  3. stirringthe mixture was stirred for 2 hours
  4. customafter which the solvent was removed by evaporation under reduced pressure
  5. addition300ml of ethyl acetate and 200 ml of water were added to the residue
  6. customThe ethyl acetate layer was separated
  7. washwashed with an aqueous solution of sodium chloride
  8. concentrationwas concentrated by evaporation under reduced pressure
  9. customThe solid obtained
  10. customwas triturated in diisopropyl ether
  11. filtrationfiltered

出典と根拠

ORDレコード
ord-eb29142027c147c19c01b94e4d842bec
出典データセット
uspto-grants-1991_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05002942

反応ノート

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