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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1288343Generated: November 3, 2026

Acetic Anhydride → N-{4-[(Oxan-2-yl)oxy]nonyl}acetamide

https://huagongshe.com/reaction/1288343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant4-(2-Tetrahydropyranyloxy)nonylamineHCID 20327684—
SolventPyridineHCID 1049—
ProductN-{4-[(Oxan-2-yl)oxy]nonyl}acetamideHCID 21503928—

Reaction Steps

To a stirred, ice cold solution of 4-(2-tetrahydropyranyloxy)nonylamine (7.29 g., 0.03 mole) in pyridine (40 ml.) is added acetic anhydride (3.06 g., 0.03 mole) at such a rate as to maintain the reaction temperature at 5°-10°C. The reaction is then allowed to stand at room temperature for 6 hours, poured into ice water (200 ml.) and extracted with ether (2 × 100 ml.). The ether is extracted with ice cold 5% hydrochloric acid (2 × 20 ml.), washed with brine (2 × 25 ml.), then dried over sodium sulfate. Evaporation in vacuo affords the subject compound as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03987091
Source datasetuspto-grants-1976_10
ORD IDord-76b123cd98964ac4b1f91c6f6c15d31a
Source noteuspto-grants-1976_10