HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromo-4-(4-chlorophenyl)-4-oxobutanoic acid → Hydrogen Bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromo-4-(4-chlorophenyl)-4-oxobutanoic acid | HCID 169666 | — |
| Reactant | HCID 21226029 | HCID 21226029 | — |
| Reactant | HCID 86739400 | HCID 86739400 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Hydrogen Bromide | HCID 260 | 296.6% |
| Product | HCID 13059235 | HCID 13059235 | — |
Reaction Steps
5-(m-Methoxybenzyl)-3,4,5,6-tetrahydro-s-triazin-2(1H) thione (2.37 g, 0.01 mole) was partly dissolved in methanol (100 ml) at 45° C. and 3-bromo-3-(p-chlorobenzoyl) propionic acid (2.92 g, 0.01 mole) dissolved in the same solvent (50 ml) was added. The temperature was held at about 45° C. until all the triazinthione dissolved, and the mixture was then allowed to stand for 3 hours. The solvent was evaporated to give a pale yellow foam, which was triturated with isopropanol to give the title compound hydrobromide hemipropanolate (2.4 g, 44%) m.p. 123°-125° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04447604 |
| Source dataset | uspto-grants-1984_05 |
| ORD ID | ord-d72a8f5ee7b24645a55c952948c7aab1 |
| Source note | uspto-grants-1984_05 |