Formaldehyde → 1-(4-Aminobutyryl)hexahydropyrmidine

HRID 362689

Reaktionsgleichung

Reaktionsgleichung von HRID 362689
NCCC[CH2:5][NH:6][CH2:7][CH2:8][CH2:9][NH2:10].C=O.[Si](=O)=O.[OH-:16].[NH4+:17].[C:18]1([CH3:24])[CH:23]=[CH:22]C=CC=1>O.CO.C(OCC)(=O)C>[NH2:17][CH2:22][CH2:23][CH2:18][C:24]([N:10]1[CH2:9][CH2:8][CH2:7][NH:6][CH2:5]1)=[O:16]

Komponenten

9

Versuchsvorschrift

To a solution of 7.5 g of spermidine in water (150 mL) in a 250 mL round bottom flask was added paraformaldehyde (1.6 g). The resulting solution was stirred at room temperature for three hours. TLC (silicon dioxide, ethyl acetate:methanol:ammonium hydroxide=3:6:1) indicated there was no S.M. (Rf-0.01). To the reaction mixture was added toluene (100 mL). The resulting heterogeneous solution was concentrated on a rotovap at 45° C. for 30 minutes. The addition of toluene (100 mL) and concentration at 45° C. was repeated for two more times. The resulting thick oil was washed with tetrahydrofuran:ethanol (10:1)(×3) (220 mL). The combined organic layers were dried with sodium sulfate, filtered and concentrated to give 8.64 g of the title compound as a crude thick oil (yield 103%).

Aufarbeitung

  1. concentrationThe resulting heterogeneous solution was concentrated on a rotovap at 45° C. for 30 minutes
  2. additionThe addition of toluene (100 mL) and concentration at 45° C.
  3. washThe resulting thick oil was washed with tetrahydrofuran:ethanol (10:1)(×3) (220 mL)
  4. dry with materialThe combined organic layers were dried with sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-425aecf5935a48a1a72dd8291d9952a4
Quelldatensatz
uspto-grants-1999_02
Patentnummer
US05869734

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