Hydrochloric Acid → 10-(4-Butylphenyl)-10H-phenoxazine

HRID 1014750ノート

反応式

HRID 1014750 の反応式
C1(C)C=CC=CC=1P(C1C=CC=CC=1C)C1C=CC=CC=1C.[CH:23]1[C:36]2[NH:35][C:34]3[C:29](=[CH:30][CH:31]=[CH:32][CH:33]=3)[O:28][C:27]=2[CH:26]=[CH:25][CH:24]=1.Br[C:38]1[CH:43]=[CH:42][C:41]([CH2:44][CH2:45][CH2:46][CH3:47])=[CH:40][CH:39]=1.CC(C)([O-])C.[Na+].Cl>C([O-])(=O)C.[Pd+2].C([O-])(=O)C.C1(C)C=CC=CC=1>[CH2:44]([C:41]1[CH:42]=[CH:43][C:38]([N:35]2[C:36]3[CH:23]=[CH:24][CH:25]=[CH:26][C:27]=3[O:28][C:29]3[C:34]2=[CH:33][CH:32]=[CH:31][CH:30]=3)=[CH:39][CH:40]=1)[CH2:45][CH2:46][CH3:47]

参加物

8

反応物 5

HCID 313Hydrochloric AcidHCID 67278PhenoxazineHCID 80271Tri-o-tolylphosphineHCID 5210591-Bromo-4-butylbenzeneHCID 23676156Sodium t-butoxide

生成物 1

HCID 2238164910-(4-Butylphenyl)-10H-phenoxazine

試薬・触媒・溶媒 2

HCID 167845palladium(II) acetate触媒HCID 1140Toluene溶媒2 回

実験手順

Palladium acetate, tri-o-tolylphosphine and toluene were charged in a three-necked round-bottomed flask, and stirred for 20 minutes at room temperature. Phenoxazine, 1-bromo-4-butylbenzene, sodium t-butoxide and toluene were added, and the mixture was heated in an oil bath and refluxed for 15 hours. After cooling, concentrated hydrochloric acid was added and the mixture was stirred for 1 hour, then, the solution was passed through a neutral alumina column. The column was washed with toluene, and the solvent was removed using a rotary evaporator, to obtain yellow solid. The solid was re-crystallized from toluene/methanol, to obtain N-(4-n-butylphenyl)phenoxazine.

後処理

  1. temperaturethe mixture was heated in an oil bath
  2. temperaturerefluxed for 15 hours
  3. temperatureAfter cooling
  4. stirringthe mixture was stirred for 1 hour
  5. washThe column was washed with toluene
  6. customthe solvent was removed
  7. customa rotary evaporator
  8. customto obtain yellow solid
  9. customThe solid was re-crystallized from toluene/methanol

出典と根拠

ORDレコード
ord-cd450df1776c4e0ebeef1ab83e9add8b
出典データセット
uspto-grants-2011_07
特許番号
US07982212B2

反応ノート

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