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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990690Generated: October 31, 2026

Trifluoroacetic acid → HCID 9815473, compound

https://huagongshe.com/reaction/990690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantDiisopropylamineHCID 7912—
ReactantEthyl isovalerateHCID 7945—
Reactanttert-Butyl bromoacetateHCID 79177—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 9815473HCID 9815473—

Reaction Conditions

Temperature0 °C

Reaction Steps

n-Butyllithium (1.6 M in hexane, 20.16 ml) was added to a stirred solution of diisopropylamine (4.52 ml) in tetrahydrofuran (60 ml) at −78° C. After 15 min, ethyl isovalerate (4.03 ml) was added and the reaction left for 1 h, before tert-butyl bromoacetate (4.78 ml) was added and the reaction allowed to warm to 0° C. After 12 h water (10 ml) was added and the solvent removed in vacuo. The resulting slurry was extracted with ethyl acetate (3×20 ml), and the combined organic extracts washed with water (2×50 ml), brine (50 ml), dried over magnesium sulphate (2 g), and the solvent removed in vacuo to yield a brown oil. The oil was dissolved in dichloromethane (60 ml) and trifluoroacetic acid (12 ml) was added and the reaction stirred for 12 h. The reaction was evaporated in vacuo and the residue azeotroped with heptane to dryness. The residue was dissolved in aqueous sodium hydroxide (2M, 40 ml) and washed with dichloromethane (2×10 ml), the aqueous layer acidified with hydrochloric acid (2M) and extracted with ethyl acetate (3×10 ml). The combined ethyl acetate extracts were washed with water (10 ml) and brine (10 ml), dried over magnesium sulphate (2 g) and evaporated to give the title compound as a brown oil (4.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06462042B1
Source datasetuspto-grants-2002_10
ORD IDord-0d58a28258df426293369bc74bfc548e
Source noteuspto-grants-2002_10