HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 13285985, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 3,4,5,6-Tetrahydrophthalic anhydride | HCID 12475 | — |
| Reactant | 5-Amino-2-chlorobenzenepropanenitrile | HCID 13285984 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13285985 | HCID 13285985 | 86% |
Reaction Steps
To a stirred slurry of 5.0 g of 3,4,5,6-tetrahydrophthalic anhydride in 5 ml. of glacial acetic acid under N2 is added 7.5 g of 3-(2-cyanoethyl)-4-chloroaniline and the mixture heated to reflux for 2 hours. The reaction mixture is cooled to room temperature, water is added together with several mls. of conc. HCl and the mixture extracted with ether. The combined ether extracts are washed with saturated brine and then dried over MgSO4. Filtration and removal of the solvent yielded 8.9 g of a brown oil. The oil is dissolved in CH2Cl2, passed through a plug of alumina, the solvent removed, and then further purified by MPLC eluting with 25% EtOAc/hexanes to yield the product as a yellow solid, m.p. 87°-97° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04439229 |
| Source dataset | uspto-grants-1984_03 |
| ORD ID | ord-a9582eacf9cd47f595008e63f2c5e554 |
| Source note | uspto-grants-1984_03 |