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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1088570Erstellt: 26. Oktober 2026

Formaldehyde → 4-Methoxycarbonyl-3-methyl-2-phenylthiazolidine

https://huagongshe.com/reaction/1088570

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormaldehydeHCID 712—
EduktPotassium CarbonateHCID 11430—
EduktSodium cyanoborohydrideHCID 5003444—
Edukt2-Phenylthiazolidine-4-carboxylic acid methyl esterHCID 14790914—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
LösungsmittelAcetonitrileHCID 6342—
Produkt4-Methoxycarbonyl-3-methyl-2-phenylthiazolidineHCID 15052257100%

Reaktionsschritte

A solution of 2.23 g of 4-methoxycarbonyl-2-phenylthiazolidine in 20 m of acetonitrile was chilled to -15° C. and, after addition of 4.3 g of 35% formalin and 1.0 g of sodium cyanoborohydride, was stirred for 30 minutes. The mixture was made acidic by addition of acetic acid under chilling with ice and, after addition of water, was made alkaline by addition of potassium carbonate. The alkaline solution was extracted with ether, and the etheral extract was dried over anhydrous sodium sulfate. The extract was placed under reduced pressure to distill of the solvent. The residue was purified by silica gel column chromatography (eluent: chloroform) to give 2.37 g of 4-methoxycarbonyl-3-methyl-2-phenylthiazolidine as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04962096
Quelldatensatzuspto-grants-1990_10
ORD IDord-37c759984a684b40bd30c6c42921caf1
Quellennotizuspto-grants-1990_10