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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607656Generated: October 29, 2026

Acetic Anhydride → HCID 86743121, compound

https://huagongshe.com/reaction/1607656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantHCID 86743122HCID 86743122—
ProductHCID 86743121HCID 86743121—

Reaction Steps

68 Parts of 4-(3'-nitro-4'-chlorobenzoyl)-amino-2,2,6,6-tetramethylpiperidine are added to 250 parts of acetic anhydride. After the addition of 21 parts of triethylamine, the suspension is stirred for 16 hours at toom temperature and then for 3 hours at 100°-110°. In order to complete precipitation of the acetyl derivative, 1500 parts by volume of cold water are added and stirred at room temperature until all the excess acetic anhydride is destroyed. The precipitate is then filtered, washed neutral with water and dried. 72 parts of 4-(3'-nitro-4'-chlorobenzoyl)-amino-1-acetyl-2,2,6,6-tetramethyl-piperidine having a melting point of 198°-200° results.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04866113
Source datasetuspto-grants-1989_09
ORD IDord-cae37c96478742fba79b28cd55e12e04
Source noteuspto-grants-1989_09