HCID 53943327, compound → HCID 67243612, compound

Participants

Reaction Steps

The title compound was prepared from phenyl N-(tert-butoxycarbonyl)-β-alaninate in a similar manner as described for 2,6-dimethylphenyl 4-aminobutanoate hydrochloride. 1H NMR (400 MHz, CDCl3): δ 7.36-7.40 (t, 2H), 7.22-7.25 (t, 1H), 7.12-7.14 (d, 2H), 4.82 (s, 3H), 3.27-3.30 (m, 2H), 2.99-3.03 (t, 2H).

Provenance & Evidence