HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-(4-Bromo-phenylamino)-3-phenyl-propionic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (4-Bromophenyl)boronic acid | HCID 79599 | — |
| Reactant | tert-butyl (2S)-2-amino-3-phenylpropanoate | HCID 6931633 | — |
| Catalyst | Cupric acetate | HCID 8895 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(4-Bromo-phenylamino)-3-phenyl-propionic acid tert-butyl ester | HCID 20779316 | — |
Reaction Steps
A mixture of L-phenylalanine tert-butyl ester (1.47 g, 6.64 mmol), 4-bromophenylboronic acid (2.67 g, 13.28 mmol), triethylamine (1.9 mL, 13.28 mmol) and copper (II) acetate (1.21 g, 6.64 mmol) in dichloromethane (50 mL) was stirred at room temperature for 24 h. The solids were removed by filtration through a pad of silica gel and the desired product was obtained by chromatography eluting with 5% ethyl acetate in hexanes. 1H NMR (CDCl3)7.2 (m, 8 H), 6.48 (d, 2 H), 4.18 (t, 2 H, H-2 and NH), 3.08 (d, 2 H), 1.35 (s, 9 H)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06887877B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-bee9f900717b414599814786dd7e1392 |
| Source note | uspto-grants-2005_05 |