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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440316Generated: October 25, 2026

Benzene → 5-(1-Hydroxypropyl)-3-phenylisoxazole

https://huagongshe.com/reaction/1440316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantTriethylamineHCID 8471—
Reactant1-Pentyn-3-olHCID 92981—
ReactantBenzamide, N-chloro-HCID 12256294—
Product5-(1-Hydroxypropyl)-3-phenylisoxazoleHCID 15180765—

Reaction Steps

Dissolved in 200 ml of benzene were 18.5 g (0.12 mol) of benzenehydroxamic acid chloride synthesized in accordance with a known process [J.Org.Chem., 45, 3916 (1980)] and 10.0 g (0.12 mole) of 1-pentyne-3-ol, followed by the dropwise addition of 18 g (0.18 mol) of triethylamine under ice cooling. After they were reacted under reflux for 10 hours, the reaction mixture was washed with water and the organic layer was dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure. .The resulting residue was purified by chromatography on a silica gel column (eluent: chloroform), whereby 5-(1-hydroxypropyl)-3-phenylisoxazole was obtained as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05498619
Source datasetuspto-grants-1996_03
ORD IDord-d645da827fc04e31b200ba66e4e69009
Source noteuspto-grants-1996_03