HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Lutidine → 3,5-Dibromosalicyl 3-butenoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | 3,5-Dibromosalicylic acid | HCID 18464 | — |
| Reactant | But-3-enoyl Chloride | HCID 10975427 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3,5-Dibromosalicyl 3-butenoate | HCID 21262206 | — |
Reaction Steps
3,5-Dibromosalicyl 3-butenoate is prepared by reaction of an acetone solution of 3-butenoyl chloride and 3,5-dibromosalicylic acid in the presence of 2,6-lutidine. The 3-butenoate ester is isolated and purified. In a second step, the desired oxirane, 3,5-dibromosalicyl 3,4-oxabutanoate, is prepared by reaction of 3,5-dibromosalicyl 3-butenoate and 3-chloroperbenzoic acid in chloroform solution. The desired oxirane is isolated and purified.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06180598B2 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-137ef8ba307b4b909a8d6201c4b20be9 |
| Source note | uspto-grants-2001_01 |