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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 635523Generated: October 30, 2026

HCID 15518231, compound → HCID 11721210, compound

https://huagongshe.com/reaction/635523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 15518231HCID 15518231—
CatalystHCID 178418406HCID 178418406—
SolventTolueneHCID 1140—
ProductHCID 11721210HCID 1172121054%

Reaction Conditions

Temperature100 °C

Reaction Steps

After 2,3-(methylenedioxy)-5-methyl-6-[3-(t-butyldimethylsiloxy)propyl]-7-benzyloxy-8-methoxy-5, 6-dihydrobenzo[c]phenanthridine (871 mg, 1.46 mmol) was dissolved in toluene (30 mL), activated manganese dioxide (4.36 g) was added to the solution. The mixture was stirred at 100° C. for 2 hours. Manganese dioxide was removed by filtration. Thereafter, the filtrate was concentrated in vacuo. The resulting residue was purified by silica gel column chromatography (eluted with 33-66% methylene chloride-hexane) to provide 2,3-(methylenedioxy)-6-[3-(t-butyldimethylsiloxy)propyl]-7-benzyloxy-8-methoxy-benzo[c]phenanthridine (457 mg, yield 54%) as colorless powders.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06187783B1
Source datasetuspto-grants-2001_02
ORD IDord-5cfa8f4cf1e34a6d9d5ee68b0c4ca458
Source noteuspto-grants-2001_02