HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → HCID 86662022, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 86662021 | HCID 86662021 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86662022 | HCID 86662022 | 73.1% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A solution of 4-(3-methylpiperazin-1-yl)benzaldehyde (1.0 g, 4.89 mmol) in methylene chloride (15 mL) was cooled to 0° C. and treated with Et3N (0.68 mL, 4.89 mmol), followed by acetyl chloride (0.34 mL, 4.89 mmol). The resulting solution was stirred at 0° C. for 20 minutes and then concentrated in vacuo. The material was purified by flash chromatography on silica gel, eluting with 0% to 5% of EtOAc/CH2Cl2, to afford 4-(4-acetyl-3-methylpiperazin-1-yl)benzaldehyde (0.88 g, 73%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09238640B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-3dddde0ba647423db20a8e6bbdeba949 |
| Source note | uspto-grants-2016_01 |