HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 21567790, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 7-amino-2,3-dihydro-1H-pyrrolo[1,2-a]benzimidazole | HCID 21567732 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 21567790 | HCID 21567790 | 67.9% |
Reaction Steps
8.65 g of 7-amino-2,3-dihydro-1H-pyrrolo[1,2-a]benzimidazole (2A00) prepared according to W. Reppe Ann. 596 (1955) p. 209 are suspended in 50 cm3 of benzene. To this suspension is added dropwise 6.2 g of acetic anhydride. The mixture is boiled for 15 min and after cooling the precipitated acetyl compound is sucked off. Recrystallization from ethanol yields 7.3 g of 7-acetylamino-2,3-dihydro-1H-pyrrolo[1,2-a]benzimidazole. Melting point: 250°-255°C. Two further recrystallizations from ethanol raise the melting point to 260°-262°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03931156 |
| Source dataset | uspto-grants-1976_01 |
| ORD ID | ord-b8da94ca87aa433f94b1593807798789 |
| Source note | uspto-grants-1976_01 |