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Phenylethanolamine → HCID 13713311, 화합물

HRID 2308740
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HRID 2308740 반응식
NCC(C1C=CC=CC=1)O.[N+](C1C=CC(CCC(C)=O)=CC=1)([O-])=O.C1(C)C=CC(S(O)(=O)=O)=CC=1.Cl.[C:37]1([CH:43]([OH:59])[CH2:44][NH:45][CH:46]([CH3:58])[CH2:47][CH2:48][C:49]2[CH:54]=[CH:53][C:52]([N+:55]([O-:57])=[O:56])=[CH:51][CH:50]=2)[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=1>O.C1(C)C=CC=CC=1>[C:37]1([CH:43]([OH:59])[CH2:44][NH:45][CH:46]([CH3:58])[CH2:47][CH2:48][C:49]2[CH:50]=[CH:51][C:52]([N+:55]([O-:57])=[O:56])=[CH:53][CH:54]=2)[CH:38]=[CH:39][CH:40]=[CH:41][CH:42]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 1000PhenylethanolamineHCID 6101p-Toluenesulfonic acidHCID 122356724-(4-Nitrophenyl)butan-2-oneHCID 13713312HCID 13713312, 화합물

생성물 1

HCID 13713311HCID 13713311, 화합물

시약·촉매·용매 2

HCID 962Water용매
HCID 1140
Toluene
용매

실험 절차

A solution of 5.0 g. (25.9 mM) of 2-amino-1-phenylethanol and 3.55 g. (25.9 mM) of methyl 2-(4-nitrophenyl)ethyl ketone in 60 ml. of toluene containing 10 mg. of para-toluenesulfonic acid was heated at reflux for six hours in a flask equipped with a Dean-Stark trap. The water that formed during the reaction was removed via the trap, and then the reaction mixture was cooled to room temperature and concentrated to dryness by evaporation of the solvent under reduced pressure. The solid product that remained was dissolved in 50 ml. of tetrahydrofuran and the solution was heated to reflux. A solution of 13.5 ml. of 2N borane-methyl sulfide complex in tetrahydrofuran was then added dropwise to the reaction mixture, and the mixture was refluxed for an additional ninety minutes. After cooling the reaction mixture to room temperature, it was diluted by addition of diethyl ether saturated with hydrogen chloride. The precipitate that formed was collected by filtration and crystallized from ethanol and diethyl ether to give 3.29 g. of 1-phenyl- 2-[1-methyl-3-(4-nitrophenyl)propylamino]ethanol hydrochloride. M.P. 203°-213° C.

후처리

  1. temperatureat reflux for six hours in a flask
  2. customequipped with a Dean-Stark trap
  3. customwas removed via the trap
  4. concentrationconcentrated to dryness by evaporation of the solvent under reduced pressure
  5. dissolutionThe solid product that remained was dissolved in 50 ml
  6. temperatureof tetrahydrofuran and the solution was heated to reflux
  7. additionof 2N borane-methyl sulfide complex in tetrahydrofuran was then added dropwise to the reaction mixture
  8. temperaturethe mixture was refluxed for an additional ninety minutes
  9. temperatureAfter cooling the reaction mixture to room temperature
  10. additionit was diluted by addition of diethyl ether saturated with hydrogen chloride
  11. customThe precipitate that formed
  12. filtrationwas collected by filtration
  13. customcrystallized from ethanol and diethyl ether
  14. customto give 3.29 g

출처 및 근거

ORD 기록
ord-a63b82efc3fa447f86a4975eed9a0f7a
출처 데이터셋
uspto-grants-1987_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04690951

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