Reaktion #2383768

ord-2f70cfc310794dc78a54f2efdc4ae944

Reaktionsgleichung

CCSCCN(C(OC(C)(C)C)C(=O)O)C(OC(C)(C)C)C(=O)O
N,N-bis-(tert-butoxycarboxy-methyl)-S-ethyl-2-mercaptoethylamine
Cl
hydrochloric acid
CCSCCN(C(O)C(=O)O)C(O)C(=O)O.Cl
N,N-Bis-(hydroxycarboxy-methyl)-S-ethyl-2-mercaptoethylamine-hydrochloride

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe resulting reaction mixture
  2. 2
    Einengenconcentrated by evaporation in a vacuum
  3. 3
    FiltrationThen, the product is filtered off
  4. 4
    Sonstigedried in a medium-high vacuum

Vorschrift

1.67 g (5 mmol) of N,N-bis-(tert-butoxycarboxy-methyl)-S-ethyl-2-mercaptoethylamine is dissolved in 12 ml of tetrahydrofuran and mixed with 6 ml of concentrated hydrochloric acid. The resulting reaction mixture is stirred for 1 hour at room temperature and concentrated by evaporation in a vacuum. The residue is pulverized with 10 ml of absolute diethyl ether. Then, the product is filtered off and dried in a medium-high vacuum.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06488909B1uspto-grants-2002_12