HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16191Generated: October 26, 2026
8-Chloro-10,11-dihydro-5H-dibenzo[b,f][1,4]diazepine → HCID 136085037, compound
https://huagongshe.com/reaction/16191
Participants
| Role | Name | HCID | Charge |
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| Reactant | 8-Chloro-10,11-dihydro-5H-dibenzo[b,f][1,4]diazepine | HCID 59343245 | — |
| Catalyst | Manganese dioxide | HCID 14801 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 136085037 | HCID 136085037 | 102.6% |
Reaction Steps
To a solution of 8-chloro-10,11-dihydro-5H-dibenzo[b,f][1,4]diazepine (8.75 g, 37.9 mmol) in CH2Cl2 (375 mL) was added MnO2 (14.5 g, 166 mmol). The reaction mixture was stirred at room temperature for 1.5 h. After filtration through dicalite, washing with CH2Cl2, the volatiles were removed in vacuo. The crude product was dissolved in ethanol (250 mL) wherafter 2N (aq) NaOH (20 mL) was added. This mixture was stirred at room temperature for 2.5 h. The reaction mixture was filtrated through dicalite and washed with CH2Cl2. After removal of the solvent under reduced pressure, the residu was dissolved in ethanol (350 mL). NaOH (2N, 20 mL) was added and the mixture was stirred for 3 h. Water was added and the mixture was extracted with ethyl acetate (3×). The combined organic layers were washed with brine, dried and evaporated to afford the title compound (8.9 g, 38.9 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07737136B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-bac32aa16a0143ae82d270190b816ba0 |
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| Source note | uspto-grants-2010_06 |
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