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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507028Generated: November 3, 2026

Sodium Chloride → 7-Methyl-8-(trifluoromethyl)-1,2,3,4-tetrahydro-5H-1-benzazepin-5-one

https://huagongshe.com/reaction/507028

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantPropan-2-yl 7-methyl-5-oxo-8-(trifluoromethyl)-2,3,4,5-tetrahydro-1H-1-benzazepine-1-carboxylateHCID 59432498—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product7-Methyl-8-(trifluoromethyl)-1,2,3,4-tetrahydro-5H-1-benzazepin-5-oneHCID 5943239580%

Reaction Steps

Heat a degassed mixture of isopropyl 7-methyl-5-oxo-8-trifluoromethyl-2,3,4,5-tetrahydrobenzo[b]azepine-1-carboxylate (6.68 g, 20.28 mmol) and sodium chloride (37.5 g) in water (7 mL) and dimethyl sulfoxide (180 mL) at reflux under nitrogen for 5 h. Dilute the cooled mixture with water (500 mL) and extract with ethyl acetate (2×300 mL). Wash the combined organic extracts with brine (200 mL), dry over anhydrous sodium sulfate and filter. Remove the solvents under reduced pressure and purify the residue by column chromatography on silica gel, eluting with ethyl acetate/hexanes (1:4), to afford the title compound as a yellow solid (3.94 g, 80%). ESI MS m/z 242 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786108B2
Source datasetuspto-grants-2010_08
ORD IDord-e7dbfbde3af6400fbcf2ccd8d969fa6d
Source noteuspto-grants-2010_08