HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Methylbenzylamine → 8-(N-Benzyl-N-methylamino)octan-1-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Methylbenzylamine | HCID 7669 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Octanol, 8-bromo- | HCID 162607 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 8-(N-Benzyl-N-methylamino)octan-1-ol | HCID 16662153 | 79% |
Reaction Steps
To a 250 mL flask was charged N-benzyl-N-methylamine (24.3 g, 200 mmol), potassium carbonate (28 g, 200 mmol), 8-bromooctan-1-ol (14 g, 67 mmol) and ACN (150 mL). This reaction mixture was stirred at 35° C. to 40° C. for 5 hours. The solid material was then filtered and the filtrate was distilled to an oil under high vacuum to remove excess N-benzyl-N-methylamine. The residue was dissolved in MTBE (150 mL) and washed with 15% ammonium chloride solution (2×100 mL), brine (100 mL), dried with 20 g of sodium sulfate, filtered and distilled under vacuum to give the title intermediate as an oil (13.2 g, 79% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07524880B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-4f88a82e8da14466a1800067a0b798a3 |
| Source note | uspto-grants-2009_04 |