4-Fluorobenzonitrile → n-(4-Cyanophenyl)alanine iso-butyl ester

HRID 411431Notes

Reaction equation

HRID 411431 reaction equation
F[C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[CH:4][CH:3]=1.Cl.[CH2:11]([O:15][C:16](=[O:20])[CH:17]([CH3:19])[NH2:18])[CH:12]([CH3:14])[CH3:13]>>[CH2:11]([O:15][C:16](=[O:20])[C@H:17]([CH3:19])[NH:18][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[CH:4][CH:3]=1)[CH:12]([CH3:14])[CH3:13]

Participants

3

Procedure

Following General Procedure AP above and using 4-fluorobenzonitrile (Aldrich) and D,L-alanine iso-butyl ester hydrochloride (from Example AA above), the title compound was prepared as an oil. The product was recovered by column chromotography on silica gel using 1:5 EtOAc/hexanes as the eluent.

Workup

  1. customThe product was recovered by column chromotography on silica gel using 1:5 EtOAc/hexanes as the eluent

Sources & evidence

ORD record
ord-377634f36b654cd59982f5679eb61593
Source dataset
uspto-grants-2003_05
Patent number
US06559141B2

Reaction notes

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