HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene, 1-(chloromethyl)-2-fluoro- → N-(2-fluorophenylmethyl)-3-hydroxy-N-methyl-3-phenylpropylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene, 1-(chloromethyl)-2-fluoro- | HCID 9580 | — |
| Reactant | 2,2,6,6-Tetramethylpiperidine | HCID 13035 | — |
| Reactant | 3-Methylamino-1-phenylpropanol | HCID 2733989 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-(2-fluorophenylmethyl)-3-hydroxy-N-methyl-3-phenylpropylamine | HCID 12951843 | 75.1% |
Reaction Steps
A mixture of 3-hydroxy-N-methyl-3-phenylpropylamine (8.3 g, 50 mM), 2,2,6,6-tetramethylpiperidine (8.4 ml, 50 mM), o-fluorobenzyl chloride (7.25 g, 50 mM) and acetonitrile (100 ml) was stirred for 24 hours at ambient temperature. The resulting precipitate was removed by filtration, the precipitate washed with acetonitrile and the combined filtrate and washings evaporated under reduced pressure. The residue was partitioned between 2N hydrochloric acid (100 ml) and ether (100 ml), the aqueous layer basified and extracted with ether (2×100 ml). The ether extract was dried and the solvent removed under reduced pressure to yield an oil (10.3 g). Distillation gave the title compound b.p. 160°-2° C./0.6 mbar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04626522 |
| Source dataset | uspto-grants-1986_12 |
| ORD ID | ord-8d869784870844408ce5698be500f924 |
| Source note | uspto-grants-1986_12 |