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Triethylamine → N-(2-ethylthioethyl)-glycine tert-butyl ester

HRID 1834874
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1834874
Cl.[CH2:2]([S:4][CH2:5][CH2:6][NH2:7])[CH3:3].C(N(CC)CC)C.Cl[CH2:16][C:17]([O:19][C:20]([CH3:23])([CH3:22])[CH3:21])=[O:18]>C(Cl)(Cl)Cl>[C:20]([O:19][C:17](=[O:18])[CH2:16][NH:7][CH2:6][CH2:5][S:4][CH2:2][CH3:3])([CH3:23])([CH3:22])[CH3:21]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 8471TriethylamineHCID 66052tert-Butyl chloroacetateHCID 30168702-(Ethylthio)ethylamine hydrochloride

Produkt 1

HCID 20372345N-(2-ethylthioethyl)-glycine tert-butyl esterAusbeute 34,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6212ChloroformLösungsmittel

Versuchsvorschrift

To a solution of 10 g of 2-ethylthioethylamine hydrochloride and 15 g of triethylamine in 20 ml of chloroform was added with stirring 11 g of tert-butyl chloroacetate over a period of 30 minutes, while maintaining the temperature at 30°-70° C. The reaction mixture was held at 70° C for an addition 1 hour. At the end of this period, the chloroform was evaporated in vacuo, and the residue was taken up in 40 ml of 2N NaOH solution and 50 ml of benzene, transferred into a separatory funnel and well shaken. The benzene solution was separated, washed with water, dried over anhydrous sodium sulfate and filtered. After evaporation of benzene, the residue was distilled under reduced pressure to give 5.3 g (34 percent) of N-(2-ethylthioethyl)glycine tert-butyl ester, B.P. 106°-9° C/1.5 mm Hg.

Aufarbeitung

  1. temperaturewhile maintaining the temperature at 30°-70° C
  2. additionThe reaction mixture was held at 70° C for an addition 1 hour
  3. customAt the end of this period, the chloroform was evaporated in vacuo
  4. custom50 ml of benzene, transferred into a separatory funnel
  5. customThe benzene solution was separated
  6. washwashed with water
  7. dry with materialdried over anhydrous sodium sulfate
  8. filtrationfiltered
  9. customAfter evaporation of benzene
  10. distillationthe residue was distilled under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-b449ad88e71d424a9c8425f317db2ed7
Quelldatensatz
uspto-grants-1978_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04071621

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