Formaldehyde → (S)-1-[4-[3-(Acetyloxy)-1-pyrrolidinyl]-2-butynyl]-2-pyrrolidinone

HRID 1710132Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1710132
[C:1]([O:4][C@H:5]1[CH2:9][CH2:8][NH:7][CH2:6]1)(=[O:3])[CH3:2].[CH2:10]([N:13]1[CH2:17][CH2:16][CH2:15][C:14]1=[O:18])[C:11]#[CH:12].[CH2:19]=O>O1CCOCC1>[C:1]([O:4][C@H:5]1[CH2:9][CH2:8][N:7]([CH2:19][C:12]#[C:11][CH2:10][N:13]2[CH2:17][CH2:16][CH2:15][C:14]2=[O:18])[CH2:6]1)(=[O:3])[CH3:2]

Komponenten

5

Edukt 3

HCID 712FormaldehydeHCID 124643131-(Prop-2-yn-1-yl)pyrrolidin-2-oneHCID 15046661acetic acid (S)-pyrrolidin-3-yl ester

Produkt 1

HCID 15046674(S)-1-[4-[3-(Acetyloxy)-1-pyrrolidinyl]-2-butynyl]-2-pyrrolidinoneAusbeute 47,9 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 312751,4-DioxaneLösungsmittel

Versuchsvorschrift

A mixture of 500 mg of (S)-3-acetoxypyrrolidine, 530 mg of N-propargyl-2-pyrrolidinone, 150 mg of paraformaldehyde and 50 mg of cupric chloride in 10 ml of dioxane was stirred at reflux under argon for 4 hours. The dioxane was evaporated, the residue was treated with 5 ml of 1N hydrochloric acid and extracted twice with ether. The aqueous acid was basified with 1 g of sodium bicarbonate and extracted twice with dichloromethane. The extracts were combined, dried, filtered and concentrated in vacuo to an oil. This oil was purified by chromatography (alumina), giving 490 mg of the desired product as a yellow oil, [α]D26 =-3° (c, 1.02, methanol).

Aufarbeitung

  1. temperatureat reflux under argon for 4 hours
  2. customThe dioxane was evaporated
  3. additionthe residue was treated with 5 ml of 1N hydrochloric acid
  4. extractionextracted twice with ether
  5. extractionextracted twice with dichloromethane
  6. customdried
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo to an oil
  9. customThis oil was purified by chromatography (alumina)

Quellen und Nachweise

ORD-Eintrag
ord-2f6d4247ef67497d98bd24fc65d53ab0
Quelldatensatz
uspto-grants-1990_08
Patentnummer
US04952600

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