HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1886971Generated: October 30, 2026
Water → 7-chloro-2,3,4,5-tetrahydro-1H-1-benzazepin-5-one
https://huagongshe.com/reaction/1886971
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 7-Chloro-1-(toluene-4-sulfonyl)-1,2,3,4-tetrahydro-benzo[b]azepin-5-one | HCID 66553764 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 7-chloro-2,3,4,5-tetrahydro-1H-1-benzazepin-5-one | HCID 22903483 | 89% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501730B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-ab8529b7d683433d9ddbdb58275697dd |
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| Source note | uspto-grants-2013_08 |
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