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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358232Generated: October 29, 2026

Acetic Acid → HCID 20449623, compound

https://huagongshe.com/reaction/358232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHCID 20449621HCID 20449621—
SolventAcetic AnhydrideHCID 7918—
ProductHCID 20449623HCID 20449623—

Reaction Steps

10 g of 2,2,6,6-tetramethyl-4-[3,3-bis-(3-tert.-butyl-6-methyl-4-hydroxyphenyl)-propionyloxy]-piperidine are stirred in 25 ml of acetic anhydride at 110° for 6 hours. The acetic acid formed and excess anhydride are then distilled off under vacuum as completely as possible. The residue is cooled down to room temperature, 100 ml of water are added and are mixed in efficiently, and the precipitate is filtered off, is washed with water and is dried. Crystallising from acetonitrile gives 1-acetyl-2,2,6,6-tetramethyl-4-[3,3-bis-(3-tert.-butyl-6-methyl-4-hydroxyphenyl)-propionyloxy]-piperidine having a melting point of 270° (optical stabiliser No. 2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04465765
Source datasetuspto-grants-1984_08
ORD IDord-745eeec8f5b3411995450ca670e9917f
Source noteuspto-grants-1984_08