HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37450Generated: October 30, 2026
Acetic Anhydride → HCID 178454361, compound
https://huagongshe.com/reaction/37450
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Maleic Anhydride | HCID 7923 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-BOC-hydrazino-5-amino pyridine | HCID 10376339 | — |
| Catalyst | Cobalt diacetate | HCID 6277 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 178454361 | HCID 178454361 | 28.3% |
Reaction Steps
To a stirred solution of 2-BOC-hydrazino-5-amino pyridine (1 equivalent) in acetone (50 ml/gm) was added maleic anhydride (1.1 equivalents). The reaction mixture was stirred at 25° for 2 hours. To the reaction mixture was added acetic anhydride (1.2 equivalents), cobalt acetate (0.007 equivalents) and triethylamine (0.3 equivalents). The reaction mixture was stirred at 60° for 2 hours. The color of the reaction began as bright yellow and ended as dark yellow. The reaction mixture was concentrated under reduced pressure to give a yellow brown oil. Flash vacuum chromatography (hexanes/ethyl acetate (8/2)) was used to isolate the product. The product was recrystallized in ether/hexane; yield 28.3%; m.p. 182°-184°. IR (KBr): 3400, 3300, 3100, 2990, 1700, 1610, 1500, 1410, 1360, 1320, 1270, 1210, 1150, 1050, 830, 750, 690 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05420285 |
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| Source dataset | uspto-grants-1995_05 |
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| ORD ID | ord-a9e1d90b102749fab1342dfcf79bf561 |
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| Source note | uspto-grants-1995_05 |
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