HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 6-(2-acetoxypropionyl)-3,4-dihydro-3-methyl-2(1H)-quinazolinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | 6-(2-Bromopropionyl)-3,4-dihydro-3-methyl-2(1H)-quinazolinone | HCID 13827166 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-(2-acetoxypropionyl)-3,4-dihydro-3-methyl-2(1H)-quinazolinone | HCID 14233047 | — |
Reaction Steps
A mixture of 6-(2-bromopropionyl)-3,4-dihydro-3-methyl-2(1H)-quinazolinone (2 g) prepared in Step 1, potassium acetate (2.64 g) and glacial acetic acid (20 ml) is refluxed for three hours. The reaction mixture is diluted with water and extracted with methylene chloride (3×50 ml) and the combined organic layers are washed with saturated aqueous sodium bicarbonate, dried, filtered and concentrated to obtain 6-(2-acetoxypropionyl)-3,4-dihydro-3-methyl-2(1H)-quinazolinone which is used in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04764512 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-67471646d3cb497f94e1a58e2084f24a |
| Source note | uspto-grants-1988_08 |