HuagongsheHuagongshe Chemistry Print Report · For research reference only
N,N,N',N'-Tetramethylmethanediamine → HCID 18987655, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N,N,N',N'-Tetramethylmethanediamine | HCID 5829 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 18987699 | HCID 18987699 | — |
| Product | HCID 18987655 | HCID 18987655 | — |
Reaction Steps
Acetic anhydride (19 mL, 21 g, 200 mmol) was added slowly to a stirring slurry of 2-(5-trifluoromethyl-2-pyridinyl)-1-(4-chlorophenyl)ethanone (12.1 g, 40.0 mmol) in bisdimethylaminomethane (22 mL, 16 g, 160 mmol) at 0° C. causing immediate solution. TLC showed complete conversion after 5 min and the mixture was partitioned between ether and water by adding these solvents and separating the layers. The organic layer was extracted with brine, dried over sodium sulfate, filtered, and evaporated under reduced pressure to obtain 13 g (99 percent of theory) of the title compound as a red oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05493024 |
| Source dataset | uspto-grants-1996_02 |
| ORD ID | ord-bd7c8c0e4011478d963414d248df50c9 |
| Source note | uspto-grants-1996_02 |