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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840963Generated: October 31, 2026

Ammonia → HCID 15549909, compound

https://huagongshe.com/reaction/840963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantMethanesulfonic AcidHCID 6395—
ReactantThioanisoleHCID 7520—
ReactantHCID 15549907HCID 15549907—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 15549909HCID 1554990986.6%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06369110B1
Source datasetuspto-grants-2002_04
ORD IDord-e3d538264beb4c3a8f7b33c8507e8e3f
Source noteuspto-grants-2002_04