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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173567Generated: October 31, 2026

Hydrochloric Acid → HCID 10542009, compound

https://huagongshe.com/reaction/1173567

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl bromodifluoroacetateHCID 69585—
Reactanttert-butyl N-((2S)-1-oxopropan-2-yl)carbamateHCID 7015728—
CatalystZincHCID 23994—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10542009HCID 1054200944%

Reaction Conditions

Temperature0 °C

Reaction Steps

tert-Butyl[(1S)-1-methyl-2-oxoethyl]carbamate (7.21 g) and ethyl bromodifluoroacetate (25.1 g) were dissolved in THF (65 mL), and the solution was added dropwise to a suspension of zinc powder (25.1 g) in THF (14 mL) at room temperature over 30 min. The suspension was heated under reflux for 30 min and cooled to 0° C. A 1 mol/L aqueous hydrochloric acid solution (200 mL) was added, and the mixture was extracted with ethyl acetate (100 mL). The extracted organic layer was washed with water (100 mL) and saturated brine (100 mL), dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane=1/10→3/10) to give the title compound as a pale-yellow oil (yield: 5.45 g, 44%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834051B2
Source datasetuspto-grants-2010_11
ORD IDord-77882d2ff9524abc8036db3fc2ff5d86
Source noteuspto-grants-2010_11