Diethyl Ether → (R)-3-((Benzyloxy)carbonyl)thiazolidine-4-carboxylic acid

HRID 35864

Reaktionsgleichung

Reaktionsgleichung von HRID 35864
[NH:1]1[CH2:8][S:7][CH2:6][C@H:2]1[C:3]([OH:5])=[O:4].CCOCC.[CH2:14]([O:21][C:22](Cl)=[O:23])[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>[OH-].[Na+]>[CH2:14]([O:21][C:22]([N:1]1[CH2:8][S:7][CH2:6][C@H:2]1[C:3]([OH:5])=[O:4])=[O:23])[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1

Komponenten

5

Versuchsvorschrift

In 94 ml of 2-N NaOH was dissolved 25 g of L-thioproline, and 20 ml of ether was added to the solution under agitation and ice-cooling. To this solution under agitation were added dropwise 38 ml of benzyloxycarbonyl chloride and 70 ml of 4-N NaOH at the same time in 30 minutes. The mixture was stirred for 2 hours at room temperature, washed with 100 ml of ether and treated with 6-N HCl to adjust pH to 2. The mixture was extracted with 200 ml and 100 ml of ethyl acetate and the ethyl acetate phase was washed 50 ml of water, dried over MgSO4 and filtered. The filtrate was concentrated until dryness under reduced pressure whereby an oily substance was obtained.

Aufarbeitung

  1. additionwas added to the solution under agitation and ice-
  2. temperaturecooling
  3. washwashed with 100 ml of ether
  4. additiontreated with 6-N HCl
  5. extractionThe mixture was extracted with 200 ml and 100 ml of ethyl acetate
  6. washthe ethyl acetate phase was washed 50 ml of water
  7. dry with materialdried over MgSO4
  8. filtrationfiltered
  9. concentrationThe filtrate was concentrated until dryness under reduced pressure whereby an oily substance
  10. customwas obtained

Quellen und Nachweise

ORD-Eintrag
ord-6a451b40f8a5463db5400fb49a3efa1b
Quelldatensatz
uspto-grants-1995_05
Patentnummer
US05411976

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