HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicamba → Methyl (4-chlorobenzoyl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicamba | HCID 3030 | — |
| Reactant | P-Chloroacetophenone | HCID 7467 | — |
| Reactant | Dimethyl Carbonate | HCID 12021 | — |
| Catalyst | Sodium Methoxide | HCID 10942334 | — |
| Product | Methyl (4-chlorobenzoyl)acetate | HCID 735885 | — |
Reaction Steps
Alternatively, MDBA may be prepared by the carbomethoxylation of a ketone. For example, 4-chloracetophenone reacts with excess dimethylcarbonate using sodium methoxide as a catalyst to produce methyl 4-chlorobenzoylacetate as described in U.S. Pat. No. 3,950,381. NMR data was consistent with the structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04863947 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-e0b77945035e41e3af77b259cf77d116 |
| Source note | uspto-grants-1989_09 |