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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2418459Generated: November 1, 2026

Acetic Anhydride → HCID 20446377, compound

https://huagongshe.com/reaction/2418459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant1-(2,2,6,6-Tetramethylpiperidin-4-yl)azepan-2-oneHCID 18551435—
CatalystSulfuric AcidHCID 1118—
ProductHCID 20446377HCID 2044637765.2%

Reaction Conditions

Temperature120 °C

Reaction Steps

A solution of 50.5 g (0.2 mole) of N-(2,2,6,6-tetramethylpiperidin-4-yl)-epsilon-caprolactam, prepared in Example 1, in 102 g of acetic anhydride with 0.2 g of sulfuric acid catalyst is heated for four hours at 120° C. At the end of this period the excess acetic anhydride is removed in vacuo. The residue is then dissolved in 200 ml of methylene chloride, washed thrice with 100 ml portions of water, then with 10% aqueous sodium bicarbonate and finally dried over anhydrous magnesium sulfate. The solvent is allowed to evaporate to give a crude product which when recrystallized from toluene:hexane (1:3) yields 38.4 g of white solid melting at 104°-108° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04472547
Source datasetuspto-grants-1984_09
ORD IDord-13be9dd6a81b4345a7b784cb112fbd16
Source noteuspto-grants-1984_09