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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165915Generated: November 1, 2026

Hydroxyamine hydrochloride → 5-{5-[2,6-Dimethyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)phenoxy]pentyl}-3-methylisoxazole

https://huagongshe.com/reaction/2165915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant5-[5-(2,6-Dimethyl-4-cyanophenoxy)pentyl]-3-methylisoxazoleHCID 14981838—
ReactantSodium Acetate TrihydrateHCID 23665404—
SolventEthanolHCID 702—
Product5-{5-[2,6-Dimethyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)phenoxy]pentyl}-3-methylisoxazoleHCID 1505729732.4%

Reaction Steps

A suspension of 7.0 g 5-[5-(2,6-dimethyl-4-cyanophenoxy)pentyl]-3-methylisoxazole, 1.8 g hydroxylamine hydrochloride and 3.5 g sodium acetate trihydrate in 40 ml 95% ethanol was heated at reflux under nitrogen for two days. The reaction mixture was filtered, concentrated in vacuo, and the residue in 50 ml acetic anhydride was heated at reflux for 3 hrs. The reaction mixture was poured over ice/10% sodium hydroxide and extracted with ether. The ether extracts were washed with water and saturated sodium bicarbonate, dried (K2CO3), concentrated and subjected to flash filtration (silica gel 60, 3:1 hexane/ethyl acetate) followed by chromatography (MPLC, silica gel 60, 3:1 hexane/ethyl acetate). The resulting product was crystallized from isopropyl acetate/hexane to give 2.7 g 5-{5-[2,6-dimethyl-4-(5-methyl-1,2,4-oxadiazol-3-yl)phenoxy]pentyl}-3-methylisoxazole, m.p. 45°-46° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04942241
Source datasetuspto-grants-1990_07
ORD IDord-47320be684d94a728233faf565f50e2b
Source noteuspto-grants-1990_07