Benzyl Chloride → HCID 485902, Verbindung

HRID 727018Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 727018
[Cl:1][C:2]1[C:20]([Cl:21])=[CH:19][C:5]2[N:6]([C@@H:10]3[O:16][C@H:15]([CH2:17][OH:18])[C@@H:13]([OH:14])[C@H:11]3[OH:12])[C:7](=[S:9])[NH:8][C:4]=2[CH:3]=1.[OH-].[NH4+].[CH2:24](Cl)[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1.C(Cl)Cl.CO>O>[CH2:24]([S:9][C:7]1[N:6]([C@@H:10]2[O:16][C@H:15]([CH2:17][OH:18])[C@@H:13]([OH:14])[C@H:11]2[OH:12])[C:5]2[CH:19]=[C:20]([Cl:21])[C:2]([Cl:1])=[CH:3][C:4]=2[N:8]=1)[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1

Komponenten

6

Edukt 4

HCID 7503Benzyl ChlorideHCID 14923Ammonium HydroxideHCID 3000467HCID 3000467, VerbindungHCID 21226129Dichloromethane methanol

Produkt 1

HCID 485902HCID 485902, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

Compound 53 (0.5 g) was dissolved in cold water (10 ml) containing concentrated ammonium hydroxide (2.5 ml). Benzyl chloride (0.5 ml) was added to this solution with stirring and the stirring continued at room temperature for 5 hours. The white solid (0.41 g) which had separated from solution was collected by filtration, washed with cold water. The solid was extracted with ethyl acetate (100 ml) and the ethyl acetate phase was dried over anhydrous Na2SO4 and then evaporated by aspirator to give a syrup. The syrup was subjected to a flash column of silica gel with CH2Cl2 --MeOH (15:1) as eluant. Fractions were collected (25 ml each) and fractions containing the desired compound were combined and evaporated to afford 54 which was crystallized from CH2C12 --MeOH (15:1), mp. 149° C., Yield 0.223 g (35.5%).

Aufarbeitung

  1. customThe white solid (0.41 g) which had separated from solution
  2. filtrationwas collected by filtration
  3. washwashed with cold water
  4. extractionThe solid was extracted with ethyl acetate (100 ml)
  5. dry with materialthe ethyl acetate phase was dried over anhydrous Na2SO4
  6. customevaporated by aspirator
  7. customto give a syrup
  8. customFractions were collected (25 ml each) and fractions
  9. additioncontaining the desired compound
  10. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-1492b8542f824bc3b35e3c01b5ff6901
Quelldatensatz
uspto-grants-1998_01
Patentnummer
US05712255

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