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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 425262Generated: October 29, 2026

Acetic Anhydride → HCID 66704013, compound

https://huagongshe.com/reaction/425262

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 66704006HCID 66704006—
ProductHCID 66704013HCID 66704013—

Reaction Steps

600 mg of 6-chloro-2-ethylamino 4-(4-nitrophenyl)quinoline (compound 2a) were added to 0.19 g of acetic anhydride. The mixture was boiled at 70° C. for 4 hours and cooled, and the acetic anhydride was removed by distillation. The residue was mixed with water, extracted with ethyl acetate and washed with water, and the product was obtained as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106204B2
Source datasetuspto-grants-2012_01
ORD IDord-f6cbee7c1f734408bc48ac35add165fa
Source noteuspto-grants-2012_01