HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1974380Generated: October 31, 2026
Hydrochloric Acid → Dimethyl [2-oxo-3-(indol-5yloxy)propyl]phosphonate
https://huagongshe.com/reaction/1974380
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethyl methylphosphonate | HCID 12958 | — |
| Reactant | HCID 16090860 | HCID 16090860 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Dimethyl [2-oxo-3-(indol-5yloxy)propyl]phosphonate | HCID 54258430 | — |
Reaction Steps
n-Butyl-lithium (21.8ml. of a 2.29M 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 (250g.) using methylene dichloride : ethyl acetate mixtures as eluant, to give dimethyl [2-oxo-3-(indol-5-yloxy)propyl]phosphonate as an oil, RF = 0.3 (ethyl acetate).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04000305 |
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| Source dataset | uspto-grants-1976_12 |
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| ORD ID | ord-924d113ba2bc4cdf9cfca8f1bbffa96a |
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| Source note | uspto-grants-1976_12 |
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