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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1730131Generated: November 2, 2026

Pyridine → HCID 22759221, compound

https://huagongshe.com/reaction/1730131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 22759289HCID 22759289—
SolventDiethyl EtherHCID 3283—
ProductHCID 22759221HCID 22759221—

Reaction Steps

A mixture of 1-(2-tetrahydropyranyloxy)-4 -hydroxy-5-(4-fluorophenoxy)-trans-2-pentene (23.6 g., 0.08 mole), acetic anhydride (9.2 g., 0.09 mole), and pyridine (7.9 g., 0.1 mole) is heated at 55°-60° for 4 hours and then at 95° for an additional 4 hours. The solution is cooled, diluted with ether and washed with ice-cold saturated sodium carbonate solution, ice water (3×) and brine, and dried over sodium sulfate. Removal of solvent under vacuum leaves the title compound as a residual orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03991106
Source datasetuspto-grants-1976_11
ORD IDord-7121118c367949c7a6dec9111230d240
Source noteuspto-grants-1976_11