HuagongsheHuagongshe Chemistry Print Report · For research reference only
Homophthalic anhydride → 2-carboxy-phenylacetic acid N-butyl-N-(2'-cyanobiphenyl-4-ylmethyl)-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Homophthalic anhydride | HCID 12801 | — |
| Reactant | 4'-Butylaminomethyl-2-cyanobiphenyl | HCID 15338353 | — |
| Reactant | Dichloromethane ether hexane | HCID 21850893 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-carboxy-phenylacetic acid N-butyl-N-(2'-cyanobiphenyl-4-ylmethyl)-amide | HCID 53942425 | — |
Reaction Steps
The starting material can be prepared, for example, as follows: A solution of 2.64 g of N-butyl-N-(2'-cyanobiphenyl-4-ylmethyl)-amine and 2.43 g of homophthalic acid anhydride in 50 ml of dioxane is heated under reflux for hour. After removal of the solvent, the residue is taken up in 100 ml of ethyl acetate and washed twice with 50 ml of water each time. After customary treatment, the organic phase yields a crude product that yields, from CH2Cl2 /ether/hexane, 2-carboxy-phenylacetic acid N-butyl-N-(2'-cyanobiphenyl-4-ylmethyl)-amide, m.p. 137°-139°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05369110 |
| Source dataset | uspto-grants-1994_11 |
| ORD ID | ord-37e2e7bed79a4351a2f556e361619812 |
| Source note | uspto-grants-1994_11 |