Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Thioanisole | HCID 7520 | — |
| Reactant | HCID 15549907 | HCID 15549907 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 15549909 | HCID 15549909 | 86.6% |
Reaction Steps
The ethyl 1-(4-methylphenylsulfonyl)-2,3-dihydro-1H-benz[b]azepine-4-carboxylate (0.63 g, 1.70 mmol) synthesized in Reference Example 4 was added to a mixture of trifluoroacetic acid (10 ml), methanesulfonic acid (0.30 g) and thioanisole (1.0 ml) which had been cooled to 0° C., and the resulting mixture was stirred at room temperature for 3.5 hours. The reaction mixture was poured into cooled aqueous ammonia and extracted twice with ethyl acetate, and the extract solution was washed twice with a saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the resulting residue was purified by a silica gel column chromatography (eluent; ethyl acetate:n-hexane=5:95) to obtain 0.32 g of ethyl 2,3-dihydro-1H-benz [b]azepine-4-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06369110B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-e3d538264beb4c3a8f7b33c8507e8e3f |
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| Source note | uspto-grants-2002_04 |
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