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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413838Generated: November 2, 2026

Triethyl phosphite → 5-Diethylphosphonomethyl-3-methylisoxazole

https://huagongshe.com/reaction/1413838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyl phosphiteHCID 31215—
Reactant5-(Chloromethyl)-3-methyl-1,2-oxazoleHCID 7131496—
SolventChloroformHCID 6212—
Product5-Diethylphosphonomethyl-3-methylisoxazoleHCID 10585698—

Reaction Steps

445 g of 5-chloromethyl-3-methylisoxazole and 674 g of triethyl phosphite are slowly heated to 150° C. and left at this temperature for 4 hours. After distillation, 546 g (69% of theory) of (3-methylisoxazol-5-yl)-methanephosphonic acid diethyl ester of boiling point 118°-121° C./0.3 mm Hg are obtained. 1H-NMR spectrum (CHCl3, with TMS as internal standard): τ=3.85 (d, J=3 Hz, 1H), 4.17 (m, J=8 Hz, 4H), 6.67 (d, J=22 Hz, 2H), 7.72 (s, 3H), 8.67 (t, J=8 Hz, 6H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04251539
Source datasetuspto-grants-1981_02
ORD IDord-2328a7143ec24e42a9b5fb95f5334c5c
Source noteuspto-grants-1981_02