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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 131359Erstellt: 26. Oktober 2026

Iodine → Ethyl 2-amino-2-cyanoacetate

https://huagongshe.com/reaction/131359

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktHeptaneHCID 8900—
EduktEthyl 2-cyano-2-(hydroxyimino)acetateHCID 6399078—
KatalysatorPlatinumHCID 23939—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelEthyl AcetateHCID 8857—
ProduktEthyl 2-amino-2-cyanoacetateHCID 288716141,1%

Reaktionsschritte

Combine ethyl cyanoglyoxylate-2-oxime (20.0 g, 141 mmol) and 5% Pt/C (2.0 g, 10% wt. load) in acetic acid (120 mL) and EtOAc (60 mL) and hydrogenate under 40 psi H2 overnight until the reaction is complete by TLC (5:1/heptane:EtOAc, I2 stain). Carefully filtered the spent catalyst using partial vacuum through glass fiber paper, and rinse with HOAc/EtOAc without allowing the cake to dry out. Concentrate the filtrate in vacuo on a rotovapor to an oil, leaving 25.5 g (96%) of crude amino-cyano-acetic acid ethyl ester as the HOAc salt. Partition a portion (13.0 g) of the HOAc salt between EtOAc (70 mL) and water (35 mL). Stir the biphasic solution and add dropwise aqueous 5N NaOH (16.5 mL) to adjust the pH to 8.0-8.2. Separate the layers, and extract the aqueous layer with more EtOAc (3×25 mL). Combine the organic layer, dry (MgSO4), filter, and concentrate the filtrate to dryness in vacuo on a rotovapor at low bath temperature (30-35° C.) to afford 5.68 g (65%) crude amino-cyano-acetic acid ethyl ester which was used immediately in the next reaction.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07384934B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-57b89e166bb64269b2551ecb9cef03d9
Quellennotizuspto-grants-2008_06