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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-Chloro-10,11-dihydro-5H-dibenzo[b,f][1,4]diazepineHCID 59343245—
CatalystManganese dioxideHCID 14801—
SolventDichloromethaneHCID 6344—
ProductHCID 136085037HCID 136085037102.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737136B2
Source datasetuspto-grants-2010_06
ORD IDord-bac32aa16a0143ae82d270190b816ba0
Source noteuspto-grants-2010_06