Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22144Generated: October 29, 2026

Hydroxylamine → 2-Di-n-propylamino-8-(4-ethylisoxazol-5-yl)-1,2,3,4-tetrahydronaphthalene

https://huagongshe.com/reaction/22144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxylamineHCID 787—
ReactantEthyl formateHCID 8025—
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium HydroxideHCID 14923—
Reactant2-(Di-n-propylamino)-8-butyryl-1,2,3,4-tetrahydronaphthaleneHCID 15233532—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
Product2-Di-n-propylamino-8-(4-ethylisoxazol-5-yl)-1,2,3,4-tetrahydronaphthaleneHCID 23373522—

Reaction Steps

Potassium t-butoxide (0.82 g; 7.3 mmol) was suspended in 100 ml of tetrahydrofuran (THF). Ethyl formate (1.0 g; 13.3 mmol) and 2-di-n-propylamino-8-butyryl-1,2,3,4-tetrahydronaphthalene (1.0 g; 3.3 mmol) in THF was added to the mixture. The resulting mixture was stirred at room temperature overnight. Hydroxylamine (1.2 g; 16.6 mmol) was added followed by sufficient water to dissolve the solid. The resulting mixture, having pH 6, was stirred at room temperature for 20 hours after which it was poured into water, and the pH was adjusted to 12 with ammonium hydroxide. The mixture was then extracted with methylene chloride. The extract was dried over sodium sulfate and evaporated. The residue was dissolved in 100 of toluene, and 100 mg of p-toluenesulfonic acid was added. The mixture then was refluxed for 1.5 hours after which it was poured into water and extracted with methylene chloride. The methylene chloride extract was dried over sodium sulfate and evaporated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05426226
Source datasetuspto-grants-1995_06
ORD IDord-0b48dd619f2a4b93b2a672614333945e
Source noteuspto-grants-1995_06