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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1053549Generated: October 29, 2026

tert-Butyl Dimethylphosphonoacetate → HCID 131736285, compound

https://huagongshe.com/reaction/1053549

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl DimethylphosphonoacetateHCID 4564495—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 71582576HCID 71582576—
Catalysttert-Butyl DimethylphosphonoacetateHCID 4564495—
CatalystPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131736285HCID 131736285134.2%

Reaction Conditions

Temperature5 °C

Reaction Steps

Potassium t-butoxide (8.66 g) was dissolved in tetrahydrofuran (50 mL) under a nitrogen atmosphere, and the solution was then cooled to approximately 5° C. Tert-butyl (dimethoxyphosphoryl)acetate (17.30 g) was added thereto at 15° C. or lower, and the mixture was stirred at 5 to 15° C. for 1 hour. (1R,5S)-3-Ethylbicyclo[3.2.0]hept-3-en-6-one (10.00 g) and tetrahydrofuran (25 mL) were further added thereto, and the mixture was stirred at 5 to 15° C. for 1.5 hours. Potassium t-butoxide (0.90 g) and tert-butyl(dimethoxyphosphoryl)acetate (1.73 g) were further added thereto, and the mixture was stirred for approximately 1 hour. Then, the reaction mixture was separated into aqueous and organic layers by the addition of toluene (85 mL) and water (40 mL). The organic layer was washed twice with water (20 mL) and then concentrated under reduced pressure to obtain tert-butyl [(1R,5S)-3-ethylbicyclo[3.2.0]hept-3-en-6-ylidene]acetate (23.09 g) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394235B2
Source datasetuspto-grants-2016_07
ORD IDord-7c386574e7a9482faa7bc59c4ac68082
Source noteuspto-grants-2016_07