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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1076175Generated: October 27, 2026

CID 406 → Dimethyl [2-oxo-3-(thiophen-2-yl)propyl]phosphonate

https://huagongshe.com/reaction/1076175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCID 406HCID 406—
ReactantDimethyl methylphosphonateHCID 12958—
ReactantMethyl thiophen-2-acetateHCID 88055—
ReactantButyllithiumHCID 178418339—
SolventAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductDimethyl [2-oxo-3-(thiophen-2-yl)propyl]phosphonateHCID 2132976312.9%

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 (3x) 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03956284
Source datasetuspto-grants-1976_05
ORD IDord-a46d2ec0aed540eaa495d169060d14d5
Source noteuspto-grants-1976_05