Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 57188019 | HCID 57188019 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 70167131 | HCID 70167131 | — |
Reaction Steps
To a mixture of cis-6-methoxy-2-methylamino-1-phenyl-1,2,3,4-tetrahydronaphthalene (3.55 g, prepared according to Process 1), triethylamine (3.12 cm3) and N,N-dimethylformamide (40 cm3) was added benzyl bromide (1.60 cm3). The mixture was warmed to 80° C. and stirred for 2 h. Upon cooling, the solvent was evaporated under reduced pressure to afford a brown oil. This was purified by column chromatography [silica, eluting with petroleum ether (b. p. 40-60° C.)-ethyl acetate (4:1)] to afford the title compound (3.52 g) as a light brown oil which solidified on standing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06410592B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-57de5bcd20104617a4723b0fde05b7c7 |
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| Source note | uspto-grants-2002_06 |
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