Reaktion #92963

ord-7c6c6c5c2879429d939127f5a9ef0417

Reaktionsgleichung

CC(C)(C)C=O
2,2-dimethylpropanal
O=C(O)CN1C(=O)CSC1=S
3-carboxymethylrhodanine
Cl
hydrochloric acid
O=C([O-])[O-].[K+].[K+]
K2CO3
CC(C)(C)C=C1SC(=S)N(CC(=O)O)C1=O
3-carboxymethyl-5-(2,2-dimethylpropylidene)rhodanine
Ausbeute 62.7%

Lösungsmittel

Reaktionsbedingungen

Temperatur
60°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionextracted with ethyl acetate
  2. 2
    SonstigeThe extract was purified through a silica gel column
  3. 3
    Sonstigerecrystallized from a mixed solvent of ethyl acetate and ethanol

Vorschrift

Into 20 ml of dry DMF was dissolved 1.5 g (0.008 mole) of 3-carboxymethylrhodanine. To the solution was added 2.2 g (0.016 mole) of K2CO3 at a room temperature, and further 1 g (0.012 mole) of 2,2-dimethylpropanal was added dropwise at 60° C. After agitating at 60° C. for 30 minutes, the reaction mixture was poured into water. The resultant was adjusted to pH 4 with a dilute hydrochloric acid and then extracted with ethyl acetate. The extract was purified through a silica gel column and recrystallized from a mixed solvent of ethyl acetate and ethanol to give 1.3 g of 3-carboxymethyl-5-(2,2-dimethylpropylidene)rhodanine in the form of light yellow needle (yield: 63%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04609736uspto-grants-1986_09