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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417331Generated: October 29, 2026

Pyridine → HCID 67600187, compound

https://huagongshe.com/reaction/1417331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactantp-Anisoyl chlorideHCID 7477—
ReactantHCID 10922371HCID 10922371—
SolventDichloromethaneHCID 6344—
ProductHCID 67600187HCID 67600187—

Reaction Conditions

Temperature-10 °C

Reaction Steps

A solution of 2.3 g of 4-[4-(1H-imidazol-1-yl)phenoxy]butaneamine (Example 2) in 50 ml of dichloromethane containing 2 ml of pyridine is treated with 2.0 g of 4-methoxybenzoyl chloride. The reaction mixture is allowed to stand at room temperature for 18 hours, and is then heated at reflux for one hour. The volatiles are removed in vacuo. The residue is partitioned between 100 ml of dichloromethane and 100 ml of water. The dichloromethane layer is dried over Na2SO4, and then heated to gentle boiling. Hexane is then added to turbidity and the mixture cooled at -10° C. A tacky precipitate results and crystals develop in the supernatant solvent. These are collected, washed with hexane, and dried in vacuo at room temperature; m.p. 125°-126° C.; yield, 0.4 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05877196
Source datasetuspto-grants-1999_03
ORD IDord-9b4a9f8b3f7443d8a06676047733f240
Source noteuspto-grants-1999_03