HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → HCID 86697212, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 84792074 | HCID 84792074 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86697212 | HCID 86697212 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
To a cooled (0° C.) solution of 2-(4-bromo-3,5-dimethylphenyl)ethanamine (100 mg) and triethylamine (68 μL) in dichloromethane (3 mL) is added acetyl chloride (31 μL). The mixture is stirred for 2 hours at 0° C. Then the mixture is partitioned between dichloromethane and water. The organic phase is separated and dried (MgSO4). The solvent is evaporated and the residue is purified by HPLC on reversed phase to give the title compound. Yield: 25 mg; LC (method 7): tR=0.98 min; Mass spectrum (ESI+): m/z=270 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08642585B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-afc9a0d1d6d44201bd5970893bb5ef2e |
| Source note | uspto-grants-2014_02 |