HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846056Generated: October 31, 2026
m-Chloroperbenzoic acid → HCID 67883980, compound
https://huagongshe.com/reaction/846056
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 67883915 | HCID 67883915 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67883980 | HCID 67883980 | — |
Reaction Steps
A solution of 3.04 g (15 mmol) of m-chloroperbenzoic acid in 30 ml of dichloromethane is added dropwise over a period of 45 minutes at -15°, with stirring, to a solution of 2.3 g (10 mmol) of (+)-(9bR*,13aR*)-2oxo-1,4,5,10,11,12,13,13a-octahydro-2H-pyrrolo[2',1':3,4]pyrazino[2,1-i]indole in 30 ml of dichloromethane. The reaction mixture is then stirred for 4 hours at -15°, then diluted with 100 ml of dichloromethane and washed in succession, while ice-cold, with sodium hydrogen sulfite solution (5%) and sodium hydrogen carbonate solution (5%). The organic phase is separated off, dried over sodium sulfate and concentrated by evaporation in vacuo. The (+)-(9bR*,13aR*)-2,7-dioxo-1,4,5,7,8,10,11,12,13,13a-decahydro-2H-pyrrolo[2',1':3,4]pyra zino[2,1-i]indole is obtained in the form of a foam, which can be further reacted without being further purified.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05135930 |
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| Source dataset | uspto-grants-1992_08 |
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| ORD ID | ord-115a2bed2c054f2fb26b77a6afbbc2d5 |
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| Source note | uspto-grants-1992_08 |
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