HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 3-(4-aminophenyl)propanoate → Ethyl 4-[15-(trifluoromethyl)pentadecylamino]hydrocinnamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 3-(4-aminophenyl)propanoate | HCID 10442595 | — |
| Reactant | 15-(Trifluoromethyl)pentadecyl bromide | HCID 12797298 | — |
| Product | Ethyl 4-[15-(trifluoromethyl)pentadecylamino]hydrocinnamate | HCID 20549401 | — |
Reaction Steps
In a manner directly analogous to that described in Example 8, ethyl 4-aminohydrocinnamate is alkylated with 15-(trifluoromethyl)pentadecyl bromide to form ethyl 4-[15-(trifluoromethyl)pentadecylamino]hydrocinnamate. Subsequently, in a manner directly analogous to that described in Example 9, ethyl 4-[15-(trifluoromethyl)pentadecylamino]hydrocinnamate is hydrolyzed to 4-[15-(trifluoromethyl)pentadecylamino]hydrocinnamic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04310545 |
| Source dataset | uspto-grants-1982_01 |
| ORD ID | ord-caeb0d65111a476c91cb2e4752760169 |
| Source note | uspto-grants-1982_01 |