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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1579495Generated: November 2, 2026

Hydrochloric Acid → Dimethyl [2-oxo-3-(indol-5yloxy)propyl]phosphonate

https://huagongshe.com/reaction/1579495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethyl methylphosphonateHCID 12958—
ReactantHCID 16090860HCID 16090860—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductDimethyl [2-oxo-3-(indol-5yloxy)propyl]phosphonateHCID 54258430—

Reaction Conditions

Temperature-78 °C

Reaction Steps

n-Butyl-lithium (21.8ml. of a 2.92M solution in hexane) was added to a solution of dimethyl methylphosphonate (6.2g.) in dry tetrahydrofuran (50ml.) at -78°C. in an atmosphere of argon. After 10 minutes, a solution of ethyl 5-indolyloxyacetate (5.5g.) in dry tetrahydrofuran (50ml.) was added dropwise, and the mixture was stirred for 2 hours at -78°C. The reaction mixture was poured into 2N hydrochloric acid and stirred vigorously for 5 minutes, then the solvents were evaporated under reduced pressure. The residue was shaken with a mixture of ethyl acetate and water, and the organic phase was separated and washed with brine. The solution was dried, the solvents were evaporated and the residue was chromatographed on a column of silica gel MFC (250 g.)using methylene dichloride : ethyl acetate mixtures as eluant, to give dimethyl [2-oxo-3-(indol-5yloxy)propyl]phosphonate as an oil, RF = 0.3 (ethyl acetate).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03931206
Source datasetuspto-grants-1976_01
ORD IDord-d288cf5d38214781a610c26636e06b95
Source noteuspto-grants-1976_01