HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5170Generated: October 23, 2026
Chloroform → Ethyl 3-oxobutyl(diethoxymethyl)phosphinate
https://huagongshe.com/en/reaction/5170
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Methyl vinyl ketone | HCID 6570 | — |
| Reactant | HCID 178418659 | HCID 178418659 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 3-oxobutyl(diethoxymethyl)phosphinate | HCID 14362820 | — |
Reaction Steps
15.0 g of ethyl trimethylsilyl(diethoxymethyl)phosphonite are added dropwise to a stirred solution of 3.9 g of methyl vinyl ketone under an atmosphere of nitrogen at room temperature. The mixture is then heated to 50° C. for a period of 1 hour. The mixture is then allowed to cool to room temperature, 25 ml of chloroform is then added followed by 10 ml water and this mixture is vigorously stirred for a period of 0.5 h. The organic layer is then separated, dried over magnesium sulphate and concentrated under reduced pressure and the crude product distilled under reduced pressure to give ethyl 3-oxobutyl(diethoxymethyl)phosphinate, b.p. 130°-135° C./0.02 mbar, 31P=+45.3 ppm (CDCl3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05243062 |
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| Source dataset | uspto-grants-1993_09 |
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| ORD ID | ord-30eae213606d47d0a395349b420efeef |
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| Source note | uspto-grants-1993_09 |
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