HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloro-2-fluoroaniline → N-(2-fluoro-4-chlorophenyl)valine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloro-2-fluoroaniline | HCID 93898 | — |
| Reactant | alpha-Cyano-m-phenoxybenzyl alpha-bromoisovalerate | HCID 13705788 | — |
| Product | N-(2-fluoro-4-chlorophenyl)valine | HCID 54022058 | — |
Reaction Steps
Following the procedure of Example 6, 2-fluoro-4-chloroaniline is reacted with m-phenoxy-α-cyanobenzyl α-bromoisovalerate to give the m-phenoxy-α-cyanobenzyl ester of N-(2-fluoro-4-chlorophenyl)valine, MS m/e 452 (M+). Alternatively 2-fluoro-4-chloroaniline is reacted with the sodium salt of α-bromoisovaleric acid to give N-(2-fluoro-4-chlorophenyl)valine, which is then esterified using m-phenoxy-α-cyanobenzyl bromide or mesylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04411912 |
| Source dataset | uspto-grants-1983_10 |
| ORD ID | ord-291d0383b24249cab1ac95ecd857a6be |
| Source note | uspto-grants-1983_10 |