HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267993Generated: October 29, 2026
Acetic Anhydride → 7-acetyloxyimino-7H-indolizino[5,6,7-ij]isoquinoline
https://huagongshe.com/reaction/267993
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 7-hydroxyimino-7H-indolizino[5,6,7-ij]isoquinoline | HCID 136353514 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 7-acetyloxyimino-7H-indolizino[5,6,7-ij]isoquinoline | HCID 54533104 | — |
Reaction Steps
Acetic anhydride (20 cc.) is added, over the course of 5 minutes, to a stirred suspension of 7-hydroxyimino-7H-indolizino[5,6,7-ij]isoquinoline (10 g.) in pyridine (100 cc.) kept at between 8° and 10° C. A brown solution is thus obtained. After stirring for 5 minutes at 10° C., the acetic acid ester crystallises. The mixture is kept at ambient temperature for a further 2 hours and then water (600 cc.) is added. The ochre-yellow crystals thus obtained are filtered off and washed copiously with water. After drying, 7-acetyloxyimino-7H-indolizino[5,6,7-ij]isoquinoline (11.0 g.), melting at 177°-179° C. with decomposition, is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03946019 |
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| Source dataset | uspto-grants-1976_03 |
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| ORD ID | ord-2926b8c41f894844b43b72690683a296 |
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| Source note | uspto-grants-1976_03 |
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