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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417953Generated: November 3, 2026

Methanol → HCID 4913174, compound

https://huagongshe.com/reaction/1417953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantDichloromethaneHCID 6344—
Reactant1-(2-Hydroxyethyl)piperazineHCID 7677—
ReactantNaphth[1,2-c]isoxazole, 3-chloro-4,5-dihydro-HCID 10987412—
SolventChloroformHCID 6212—
SolventEthyl AcetateHCID 8857—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 4913174HCID 4913174—

Reaction Steps

A stirred mixture of 3-chloro-4,5-dihydronaphth[1,2-c]isoxazole (3.0 g, 14.63 mmol), 1-(2-hydroxyethyl)-piperazine (17.95 ml, 146.3 mmol) and K2O3 (4.1 g, 29.3 mmol) in 18 ml of N-methlypyrrolidinone under N2 was lowered into an oil bath preheated to 150° C. The mixture was heated while stirring under N2 for 1 hour. At that time, TLC (CH2Cl2) showed no remaining starting material. The mixture was removed from the heating bath, allowed to cool to room temperature, and diluted with H2O. Upon the addition of heptane, a solid precipitated. The solid was collected, washed with heptane and H2O, and dried in vacuo (0.1 mm) at 85° C. overnight to provide pure product, mp of 137°-138° C., homogeneous by TLC [silica, 1:1 CH3OH:EtOAc, Rf=0.67]. The IR (CHCl3), NMR (CDCl3) and Mass Spectrum (M+ =299, EI, 70 eV) were consistent with the structure. The yield was 2.603 g (8.70 mmol, 59.47%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05880121
Source datasetuspto-grants-1999_03
ORD IDord-6ae06f99a1ef49eab72a6fedc884439a
Source noteuspto-grants-1999_03