HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934790Generated: November 1, 2026
Benzoyl Peroxide → 10,11-Dihydro-10-hydroxy-5H-dibenz[b,f]azepine-5-carbonitrile
https://huagongshe.com/reaction/1934790
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | Chlorobenzene | HCID 7964 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 10,11-Dihydro-5H-dibenzo[b,f]azepine-5-carbonitrile | HCID 11160338 | — |
| Solvent | Water | HCID 962 | — |
| Product | 10,11-Dihydro-10-hydroxy-5H-dibenz[b,f]azepine-5-carbonitrile | HCID 9942773 | 52.2% |
Reaction Steps
190 ml of chlorobenzene and 25 g of (I) are loaded into a 500 ml pyrex round-bottom flask, under nitrogen. Afterwards, 21.2 g of N-bromosuccinimide and 2.2 g of dibenzoylperoxide are added and the mixture is heated to 85-90° C., keeping this temperature for 1.5 hours. 150 ml of water and 5 g of PEG 6000 are added, heating to 85°-90° C. for 2 hours. After decanting at 60° C., water is removed and the organic phase is washed with further water (2×100 ml). Chlorobenzene is evaporated off under vacuum at 5 mm/Hg and the residue is taken up with 50 ml of ethyl acetate. The mixture is cooled to 0° C. for 2 hours, filtered and dried at 60° C. for 4 hours, to obtain 14 g of (VI), m.p. 111-112° C., with good purity.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06384217B1 |
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| Source dataset | uspto-grants-2002_05 |
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| ORD ID | ord-0e85edefc5be4c85824275ffef2c5e78 |
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| Source note | uspto-grants-2002_05 |
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