HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934787Generated: October 31, 2026
Water → 10,11-Dihydro-10-hydroxy-5H-dibenz[b,f]azepine-5-carbonitrile
https://huagongshe.com/reaction/1934787
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 10,11-Dihydro-5H-dibenzo[b,f]azepine-5-carbonitrile | HCID 11160338 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 10,11-Dihydro-10-hydroxy-5H-dibenz[b,f]azepine-5-carbonitrile | HCID 9942773 | 61% |
Reaction Steps
13.2 g (0.060 mols) of (I) are dissolved at room temperature in 80 ml of CH2Cl2 under stirring, then 11.8 g (0.066 mols) of N-bromosuccinimide of purity above 98% and 0.70 g (0.003 mols) of di-tert-butyl-peroxalate are added under stirring. The reaction mixture is subjected to mild nitrogen stream for 5 minutes, then heated to 45° C. and stirred at this temperature for 85 minutes. The resulting suspension is added with 100 ml of demineralized water and 3 grams of polyethylene glycol with average molecular weight 400, then refluxed for 5 hours under strong stirring. After decanting at 30° C., the organic phase is separated, dried over 4 g of Na2SO4, filtered and the resulting solution is concentrated to 20 ml, added with 10 ml of hexane, cooled to 0-5° C. for 2 hours and filtered to obtain 8.64 g (61%) of (VI), m.p. 110-112° C.
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-7b11128e608e46afb61471f705308dd8 |
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| Source note | uspto-grants-2002_05 |
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