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

HRID 359775
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HRID 359775 반응식
[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
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

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

생성물 1

HCID 23449966-Phenoxybenzo[d]thiazol-2-amine수율 65.3%

시약·촉매·용매 1

HCID 176Acetic Acid용매

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온도
15 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-eb29142027c147c19c01b94e4d842bec
출처 데이터셋
uspto-grants-1991_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05002942

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