HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 4-bromobutyrate → Ethyl 4-(6-methoxybiphenyl-3-yl)aminobutyrate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 4-bromobutyrate | HCID 76300 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Methoxy-3-phenylaniline | HCID 123541 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Ethyl 4-(6-methoxybiphenyl-3-yl)aminobutyrate | HCID 20298363 | — |
Reaction Steps
29.5 g of 5-amino-2-methoxybiphenyl, 19.2 g of ethyldiisopropylamine and 28.9 g of ethyl 4-bromobutyrate are heated together (while stirring) for 4 hours at 125°. After cooling, the resulting reaction product is stirred with diethyl ether and filtered from the precipitated salt. The residue (remaining after evaporating off the ether) is recrystallized from isopropyl alcohol to obtain 22.5 g (48.5% of theory) of ethyl 4-(6-methoxybiphenyl-3-yl)amiobutyrate, MP 71° to 72.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04243678 |
| Source dataset | uspto-grants-1981_01 |
| ORD ID | ord-27be8e6e888b4915a49a0e136fae22c4 |
| Source note | uspto-grants-1981_01 |