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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1052905Generated: October 25, 2026

Hydrochloric Acid → Ethyl 2-(acetyloxy)-2-(diethyl phosphono)acetate

https://huagongshe.com/reaction/1052905

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantEthyl phosphite, (C2H5O)2(OH)PHCID 12977—
ReactantEthyl oxoacetateHCID 70211—
SolventTolueneHCID 1140—
ProductEthyl 2-(acetyloxy)-2-(diethyl phosphono)acetateHCID 413103850.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

Ethyl 2-oxoacetate (50%) (74 g, 724.8 mmol, 1.0 eq.) was added dropwise with stirring at 0° C. to a solution of diethyl hydrogen phosphite (50 g, 362.1 mmol, 1.0 eq.) in toluene (100 mL), under nitrogen. Et3N (110 g, 1.1 mol, 3.0 eq.) was added dropwise with stirring at 0° C. The resulting solution was stirred for 1 hour at room temperature. To the mixture was added acetic anhydride (37 g, 362.4 mmol, 1.0 eq.) dropwise with stirring at 0° C. The resulting solution was stirred overnight at room temperature. The pH value of the solution was adjusted to 6 with 2N HCl. The resulting solution was extracted with DCM (3×150 mL) and the organic layers were combined, dried over Na2SO4, and concentrated under vacuum. The residue was loaded onto a silica gel column with EtOAc:hexanes (1:2˜1:5) to yield the title compound (52 g) as a light yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388145B2
Source datasetuspto-grants-2016_07
ORD IDord-746b243ccbb645faabdc55b7f718fe1c
Source noteuspto-grants-2016_07