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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389236Generated: October 30, 2026

Water → 7-chloro-2,3,4,5-tetrahydro-1H-1-benzazepin-5-one

https://huagongshe.com/reaction/2389236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSulfuric AcidHCID 1118—
ReactantSodium HydroxideHCID 14798—
Reactant7-Chloro-1-(toluene-4-sulfonyl)-1,2,3,4-tetrahydro-benzo[b]azepin-5-oneHCID 66553764—
SolventTolueneHCID 1140—
Product7-chloro-2,3,4,5-tetrahydro-1H-1-benzazepin-5-oneHCID 2290348389%

Reaction Conditions

Temperature25 °C

Reaction Steps

7-Chloro-1-p-toluenesulfonyl-2,3,4,5-tetrahydro-1H-1-benzazepin-5-one (5 g) is added to 90% (w/w) sulfuric acid (50 ml), and the mixture is stirred at 0° C. to 10° C. for 2.5 hours. The reaction mixture is added to a cool water (50 mL) and then is neutralized by gradually adding thereto a solution of sodium hydroxide (75 g) in an appropriate amount of water with attention to exothermal reaction. The reaction mixture is cooled to 25° C., and the resulting yellowish green suspension is extracted with toluene (50 mL), and the organic layer is separated, washed with water (25 ml×2) and dried over sodium sulfate. After filtering off sodium sulfate, the filtrate is concentrated under reduced pressure to give a pale yellow crystals. The crystals are subjected to azeotropic dehydration with toluene in order to remove a slight amount of water to give 7-chloro-2,3,4,5-tetrahydro-1H-1-benzazepin-5-one having a moisture content of less than 100 ppm (2.5 g, yield 89%, M.p. 103-104° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273735B2
Source datasetuspto-grants-2012_09
ORD IDord-cdda269268ad4f248c7d8c602a46628a
Source noteuspto-grants-2012_09