HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → HCID 136268161, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 178499081 | HCID 178499081 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 136268161 | HCID 136268161 | 97.8% |
Reaction Steps
In a round-bottomed flask, methyl 2-(2-bromobenzyl)-5,6-dihydroxypyrimidine-4-carboxylate (300 mg, 885 μmol) was combined with DCM (10 ml) to give a brown suspension. Acetyl chloride (1M in DCM) (2.21 ml, 2.21 mmol) was added slowly at room temperature. The mixture was stirred for one hour and then poured onto aqueous saturated NH4Cl solution and extracted with DCM. The organic phase was washed with brine solution, dried (Na2SO4), and evaporated to dryness under reduced pressure. Chromatography (SiO2; DCM) provided the title product as a white solid (0.33 g; 97%). LCMS: m/z=381/383 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08921388B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-348d6041967e4111974032b3d273aaff |
| Source note | uspto-grants-2014_12 |