HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 21276160, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 21276156 | HCID 21276156 | — |
| Product | HCID 21276160 | HCID 21276160 | — |
Reaction Steps
Cyclohepta[1,2-c]pyridine, N-oxide (24.00 g, 0.147 mole) was added portionwise to a stirred solution of acetic anhydride (140 ml). The resulting yellow mixture was then stirred for 2 hours at its reflux temperature and overnight at room temperature. Excess acetic anhydride was removed by evaporation at ~55° C. on a rotary evaporator and the dark brown, oily residue was distilled (170°, 0.03 mm) and chromatographed on silica gel eluting with a mixture of ethyl acetate in methylene chloride (1:4) to give the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04803210 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-1bdd40be5e674f7db52ca7111d5dd5cf |
| Source note | uspto-grants-1989_02 |