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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1381503Generated: November 1, 2026

Acetic Anhydride → HCID 21276160, compound

https://huagongshe.com/reaction/1381503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 21276156HCID 21276156—
ProductHCID 21276160HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04803210
Source datasetuspto-grants-1989_02
ORD IDord-1bdd40be5e674f7db52ca7111d5dd5cf
Source noteuspto-grants-1989_02