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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1500255Generated: October 30, 2026

Tetrahydrofuran → HCID 66868250, compound

https://huagongshe.com/reaction/1500255

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant4-MorpholinoacetophenoneHCID 38362—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantTrimethylphosphonoacetateHCID 53413272—
SolventHydrochloric AcidHCID 313—
ProductHCID 66868250HCID 6686825069.9%

Reaction Steps

To a chilled (0° C.) solution of potassium tert-butoxide (1.0 M, 37.1 mL) was dropwise added a solution of trimethylphosphonoacetate, keeping the temperature below 25° C. The solution was then allowed to warm to room temperature and stirred for an additional five minutes, after which a solution of 4-morpholinoacetophenone in THF (20 mL) was added in one portion. The solution was slowly heated to 60° C. for 36 hours. The solution was cooled to room temperature, then diluted with a 1.0N HCl solution (100 mL), and extracted with ethyl acetate (2×100 mL). The organic layers were combined and dried over MgSO4, filtered, and the filtrate concentrated to a white solid which was recrystallized from hexane/ethyl acetate to give 3.33 grams of 3-(4-morpholinophenyl)but-2-enoic acid methyl ester intermediate (69.9% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206143B2
Source datasetuspto-grants-2015_12
ORD IDord-fa14cb7e2aae49b28f8443e3b630df80
Source noteuspto-grants-2015_12