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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52840Generated: October 26, 2026

Chloromethyl Methyl Ether → Methyl 3-(Methoxymethoxy)-5-isoxazole Carboxylate

https://huagongshe.com/reaction/52840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178498603HCID 178498603—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 3-(Methoxymethoxy)-5-isoxazole CarboxylateHCID 1893964778%

Reaction Steps

A solution of 2.0 g (14.0 mmol) of methyl 3-hydroxy-5-isoxazole carboxylate and 29.2 ml (16.8 mmol) of N,N-diisopropylethylamine in 20 ml of tetrahydrofuran was treated with 1.27 ml of chloromethyl methyl ether. After being stirred at ambient temperature for 2 h, the solution was diluted with dichloromethane, washed with water, dried over MgSO4, and concentrated in vacuo. Silica gel chromatography of the residue using 10% methanol in dichloromethane provided 129.6 mg (78%) of the desired compound as a white solid. 1H NMR (CDCl3) δ 3.57 (s, 3H), 3.96 (s, 3H), 5.37 (s, 2H), 6.64 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616714
Source datasetuspto-grants-1997_04
ORD IDord-57d4d0d7196d43deaaa29145a5863f70
Source noteuspto-grants-1997_04