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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600295Generated: October 29, 2026

(S)-Tert-butyl (1-cyano-2-(4-iodophenyl)ethyl)carbamate → (S)-2-amino-3-(4-iodophenyl)propanenitrile

https://huagongshe.com/reaction/600295

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-Tert-butyl (1-cyano-2-(4-iodophenyl)ethyl)carbamateHCID 57999650—
SolventFormic AcidHCID 284—
Product(S)-2-amino-3-(4-iodophenyl)propanenitrileHCID 5799965287.9%

Reaction Conditions

Temperature50 °C

Reaction Steps

(S)-tert-Butyl 1-cyano-2-(4-iodophenyl)ethylcarbamate (1.4 g) and formic acid (3 mL) were combined and heated at 50° C. for 10 min. Solvent was removed in vacuo and crude material was loaded onto an SCX cartridge. Non-basic impurities were washed off with methanol, then product was eluted with 10% ammonia in methanol. Solvent was removed in vacuo to give (S)-2-amino-3-(4-iodophenyl)propanenitrile (0.900 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902181B2
Source datasetuspto-grants-2011_03
ORD IDord-33b7933a967f44bb89bb2a906656a63b
Source noteuspto-grants-2011_03