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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129322Generated: October 27, 2026

Diisopropylamine → ethyl (Z)-2-Fluoro-4,4-dimethylpent-2-enoate

https://huagongshe.com/reaction/129322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantPivalaldehydeHCID 12417—
ReactantTriethyl 2-fluoro-2-phosphonoacetateHCID 2734865—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Productethyl (Z)-2-Fluoro-4,4-dimethylpent-2-enoateHCID 86745858—

Reaction Conditions

Temperature0 °C

Reaction Steps

n-Butyllithium (4.8 ml of a 1.6M solution in hexane) was added to a stirred solution of diisopropylamine (1.1 ml) in tetrahydrofuran (15 ml) at 0° C. under nitrogen. The resulting mixture was maintained at 0° C. for 0.5 hour and then cooled to -70° when a solution of ethyl diethylphosphonofluoroacetate (1.7 g) in tetrahydrofuran (5 ml) was added. After a further 0.5 hour at -70° trimethylacetaldehyde (0.76 ml) was added neat and the resulting mixture was allowed to warm to room temperature over 5 hours. After this time, water (5 ml) was added and the bulk of the solvent was removed under reduced pressure. The residue was partitioned between diethyl ether and water. The organic phase was separated, washed with water, 10% hydrochloric acid solution and brine before drying over anhydrous magnesium sulphate. The solvent was removed in vacuo to leave ethyl (Z)-2-Fluoro-4,4-dimethylpent-2-enoate as a pale green oil (1.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05466710
Source datasetuspto-grants-1995_11
ORD IDord-962f0bc3be07474ca63006da5599fa24
Source noteuspto-grants-1995_11