Acetic Acid → HCID 54394222, Verbindung

HRID 2248121Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2248121
[Cl:1][C:2]1[CH2:3][N:4]=[CH:5][C:6]2([CH3:20])[CH:17]([CH3:18])[CH:15]3[CH2:16][C:10]4=[C:11]([N:14]3[CH3:19])[CH2:12][CH2:13][C:7]2=[C:8]4[CH:9]=1.C(O)(=O)C.C([BH3-])#N.[Na+].[OH-].[Na+]>O>[Cl:1][C:2]1[CH2:3][NH:4][CH2:5][C:6]2([CH3:20])[CH:17]([CH3:18])[CH:15]3[CH2:16][C:10]4=[C:11]([N:14]3[CH3:19])[CH2:12][CH2:13][C:7]2=[C:8]4[CH:9]=1

Komponenten

6

Edukt 4

HCID 176Acetic AcidHCID 14798Sodium HydroxideHCID 5003444Sodium cyanoborohydrideHCID 53780973HCID 53780973, Verbindung

Produkt 1

HCID 54394222HCID 54394222, VerbindungAusbeute 69 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

To a stirred solution of 1.50 g of 10-chloro-1,2,3,4,5,6-hexahydro-3,6,12-trimethyl-2,6-methano-9H-pyrrolo[3,2-h][3]benzazocine and 14 ml of acetic acid, cooled to 15° C. under nitrogen, was added, 1.00 g of sodium cyanoborohydride, with stirring. The reaction mixture was stirred an additional 6.75 hr and water was added. The solution was made basic (pH 12) with 50% aqueous sodium hydroxide solution. The mixture was extracted with ether and the combined organic layers were washed with brine, dried over anhydrous potassium carbonate and filtered. The filtrate was concentrated. The residue was dissolved in 15 ml acetic acid and, as above, treated with 1.63 g of sodium cyanoborohydride for 5 hr. The residue was purified by flash column chromatography (silica gel, 2% triethylamine/0-10% methanol/ether) to afford 1.04 g (69%) of product. Recrystallization from ether-dichloromethane afforded the analytical sample, mp 168°-170° C.

Aufarbeitung

  1. additionwas added
  2. extractionThe mixture was extracted with ether
  3. washthe combined organic layers were washed with brine
  4. dry with materialdried over anhydrous potassium carbonate
  5. filtrationfiltered
  6. concentrationThe filtrate was concentrated
  7. dissolutionThe residue was dissolved in 15 ml acetic acid
  8. additionas above, treated with 1.63 g of sodium cyanoborohydride for 5 hr
  9. customThe residue was purified by flash column chromatography (silica gel, 2% triethylamine/0-10% methanol/ether)

Quellen und Nachweise

ORD-Eintrag
ord-d28ca49aba6444a4920e490b80e855d4
Quelldatensatz
uspto-grants-1991_08
Patentnummer
US05037985

Notizen zur Reaktion

Wird geladen…