HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Malonate → Diethyl-4-[4'-(4""-trifluoromethyl-phenoxy)-phenoxy]-2-pentenoyl-malonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Reactant | 4-[4-(4-Trifluoromethylphenoxy)phenoxy]-2-pentenoic acid | HCID 157794 | — |
| Product | Diethyl-4-[4'-(4""-trifluoromethyl-phenoxy)-phenoxy]-2-pentenoyl-malonate | HCID 57188560 | 87% |
Reaction Steps
One proceeds in an analogous manner to the process disclosed in Example 4 by reacting 4-[4'-(4"-trifluoromethyl-phenoxy)-phenoxy]-2-pentenoic acid at first with 12 g of pivaloyl chloride and thereafter with diethyl-ethoxy-magnesium malonate prepared from 17.6 g of diethyl malonate. The reaction mixture is worked up. 43 g of the viscous oily desired compound are obtained which turns to a faint yellow crystalline product on standing. Mp.: 52°-55° C., yield 87%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04765825 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-1008a01291634950816d178f46370320 |
| Source note | uspto-grants-1988_08 |