Hydrochloric Acid → 2-(Naphthalen-2-yl)ethan-1-amine--hydrogen chloride (1/1)

HRID 412686

Reaktionsgleichung

Reaktionsgleichung von HRID 412686
[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[CH2:11][CH2:12]O.C1(P([N:28]=[N+]=[N-])(C2C=CC=CC=2)=O)C=CC=CC=1.CCCCCCC=CCCC.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[ClH:61]>CN(C=O)C.O.C(OCC)C.C(O)C>[ClH:61].[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[CH2:11][CH2:12][NH2:28]

Komponenten

10

Reaktionsbedingungen

Temperatur
65 °C

Versuchsvorschrift

A solution comprising 2-naphth-2-ylethanol (0.5 g, 2.9 mmol) in dry DMF (5 mL) was combined under nitrogen with diphenylphosphoryl azide (0.74 mL, 3.42 mmol) and 1,8-diazaabicyclo[5.4.0]undec-7-ene (0.47 mL. 3.14 mmol). The mixture was heated at 65° C. for 3 hours and then partitioned between water and diethyl ether. The aqueous layer was separated and extracted with diethyl ether. The combined organic layers were washed with 3N hydrochloric acid and then saturated sodium bicarbonate, dried (MgSO4), filtered and concentrated by rotary evaporation. The residue was dissolved in THF (5 mL) and the solution was combined with triphenylphosphine (1 g, 3.81 mmol), stirred for 2 hours at room temperature, diluted with water (0.100 mL), stirred 3 hours, diluted with concentrated hydrochloric acid (0.33 mL) to give a precipitate, treated with ethanol (5 mL) to dissolve the precipitate and treated with diethyl ether, added slowly, to give a white precipitate. The while precipitate was isolated by filtration, washed with diethyl ether and dried under vacuum to provide 2-naphth-2-ylethylamine hydrochloride (0.447 g, 75% yield);

Aufarbeitung

  1. custompartitioned between water and diethyl ether
  2. customThe aqueous layer was separated
  3. extractionextracted with diethyl ether
  4. washThe combined organic layers were washed with 3N hydrochloric acid
  5. dry with materialsaturated sodium bicarbonate, dried (MgSO4)
  6. filtrationfiltered
  7. concentrationconcentrated by rotary evaporation
  8. dissolutionThe residue was dissolved in THF (5 mL)
  9. stirringstirred 3 hours
  10. customto give a precipitate
  11. dissolutionto dissolve the precipitate
  12. additionadded slowly
  13. customto give a white precipitate
  14. customThe while precipitate was isolated by filtration
  15. washwashed with diethyl ether
  16. customdried under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-1a3a1128779f4d53976593e7f3408b57
Quelldatensatz
uspto-grants-2003_05
Patentnummer
US06562854B2

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