HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromoacetyl chloride → 6-(Bromoacetyl)-3,4-dihydro-2(1H)-quinazolinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromoacetyl chloride | HCID 89602 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 1,2,3,4-Tetrahydroquinazolin-2-one | HCID 12360756 | — |
| Solvent | Carbon Disulfide | HCID 6348 | — |
| Product | 6-(Bromoacetyl)-3,4-dihydro-2(1H)-quinazolinone | HCID 13827162 | — |
Reaction Steps
Bromoacetyl chloride (6.2 g) is added dropwise to a stirring mixture of 3,4-dihydro-2(1H)-quinazolinone (2.6 g) and anhydrous aluminum chloride (6.3 g) in carbon disulfide (60 ml). The reaction mixture is stirred under reflux for 4.5 hours, the carbon disulfide decanted, and the residue treated with HCl (6N). The resulting solid is poured into ice water, filtered, the filtered solid washed with water and dried in vacuo, affording the desired product, which is used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04666913 |
| Source dataset | uspto-grants-1987_05 |
| ORD ID | ord-21cb6f0bea814de4b3d7bfa5f078e69d |
| Source note | uspto-grants-1987_05 |