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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350446Generated: October 31, 2026

Iodine → Ethyl 2-amino-2-cyanoacetate

https://huagongshe.com/reaction/1350446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantHeptaneHCID 8900—
ReactantEthyl 2-cyano-2-(hydroxyimino)acetateHCID 6399078—
CatalystPlatinumHCID 23939—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
ProductEthyl 2-amino-2-cyanoacetateHCID 288716141.1%

Reaction Steps

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 (1 6.5 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214673B2
Source datasetuspto-grants-2007_05
ORD IDord-bab43f0cc0214125bfb6d26db361e83e
Source noteuspto-grants-2007_05