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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395095Generated: November 2, 2026

Di-tert-butyl peroxide → HCID 20566760, compound

https://huagongshe.com/reaction/1395095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDi-tert-butyl peroxideHCID 8033—
ReactantDiethylphosphiteHCID 3780918—
ReactantHCID 20566762HCID 20566762—
ProductHCID 20566760HCID 20566760—

Reaction Conditions

Temperature150 °C

Reaction Steps

Over a 60 minute period, a solution of the above-prepared N-allylsulfonamide (24.60 g, 0.10 mole) and diethylphosphite (15 g) was added dropwise concurrently with a solution of di-t-butyl peroxide (0.90 g) in diethylphosphite (5 g) to diethylphosphite (80 g) being stirred at 150° C. with an argon purge. The resulting mixture was stirred for an additional 1 hour under these conditions. The excess diethylphosphite was distilled at 10-20 torr and the residue fractionally distilled to give 19.64 g (b.p. 150°-153° C. at 0.20 torr) of the desired compound, diethyl 3-(N-butyltrifluoromethanesulfonamido)propanephosphonate. A mixture of the phosphonate prepared in above (15.36 g, 0.040 mole) and bromotrimethylsilane (13.46 g. 0.088 mole) was stirred under a reflux condensor and calcium chloride drying tube for 96 hours. Then water (75 ml) was added and the resulting mixture stirred for 15 minutes followed by extraction with three 50 ml portions of diethylether. The ether portions were combined, dried with MgSO4 and evaporated in vacuo to give 12.25 g of the desired compound, 3-(N-butyltrifluoromethanesulfonamidopropanephosphonic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04202706
Source datasetuspto-grants-1980_05
ORD IDord-c275f46ca9d0431bb8f261fce53ca4c0
Source noteuspto-grants-1980_05