HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867125Generated: October 26, 2026
CID 406 → Dimethyl [2-oxo-3-(thiophen-2-yl)propyl]phosphonate
https://huagongshe.com/reaction/867125
Participants
| Role | Name | HCID | Charge |
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| Reactant | CID 406 | HCID 406 | — |
| Reactant | Dimethyl methylphosphonate | HCID 12958 | — |
| Reactant | Methyl thiophen-2-acetate | HCID 88055 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Dimethyl [2-oxo-3-(thiophen-2-yl)propyl]phosphonate | HCID 21329763 | 12.9% |
Reaction Steps
A solution of 37.2 g (0.3 mole) dimethyl methylphosphonate (Aldrich) in 400 ml dry tetrahydrofuran was cooled to -78° in a dry nitrogen atmosphere. To the stirred phosphonate solution was added 194 ml of 1.6 M n-butyllithium in hexane solution (Alfa Inorganics, Inc.) dropwise over a period of 18 minutes at such a rate that the reaction temperature never rose above -65°. After an additional 5 minutes stirring at -78°, 23.4 g (0.15 mole) methyl 2-(2-thienyl)acetate was added dropwise at a rate that kept the reaction temperature less than -70° (20 minutes). After 3.5 hours at -78° the reaction mixture was allowed to warm to ambient temperature, neutralized with 6 ml acetic acid and rotary evaporated to a white gel. The gelatinous material was taken up in 75 ml water, the aqueous phase extracted with 100 ml portions of chloroform (3× the combined organic extracts were backwashed (50 ml H2O), dried (MgSO4), and concentrated (water aspirator) to a crude residue and distilled, b.p. 150°-52° (<0.5 mm) to give 4.8 g dimethyl 2-oxo-3(2-thienyl)propylphosphonate (2a).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04102894 |
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| Source dataset | uspto-grants-1978_07 |
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| ORD ID | ord-5f5f245b2c534b698a0231f1227708ec |
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| Source note | uspto-grants-1978_07 |
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