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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413839Generated: October 29, 2026

Triethyl phosphite → Diethyl (3-ethylisoxazol-5-yl)-methanephosphonate

https://huagongshe.com/reaction/1413839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethyl phosphiteHCID 31215—
Reactant5-(Chloromethyl)-3-ethyl-1,2-oxazoleHCID 12364600—
ProductDiethyl (3-ethylisoxazol-5-yl)-methanephosphonateHCID 1252006871.5%

Reaction Steps

15 g of 5-chloromethyl-3-ethyl-isoxazole and 18 g of triethyl phosphite are slowly heated to 150° C. and left at this temperature for 21/2 hours. After the mixture has cooled, it is distilled under reduced pressure. 18.2 g of (3-ethylisoxazol-5-yl)-methanephosphonic acid diethyl ester of boiling point 120°-121° C./0.2 mm Hg are obtained. Yield: 71.2%. 1H-NMR spectrum (CDCl3, with TMS as internal standard): τ=3.85 (d, J=3 Hz, 1H), 4.17 (m, J=Hz, 4H), 6.60 (d, H=20 Hz, 2H), 7.35 (q, J=Hz, 2H), 8.50-8.93 (m, 9H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04251539
Source datasetuspto-grants-1981_02
ORD IDord-dc104682bbd94ab0860d0fec1ee931ec
Source noteuspto-grants-1981_02