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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2226221Generated: October 31, 2026

Hydrochloric Acid → HCID 12809805, compound

https://huagongshe.com/reaction/2226221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisopropylamineHCID 7912—
ReactantHexaneHCID 8058—
ReactantEthyl AcetateHCID 8857—
Reactanttert-butyl N-[(2S)-4-methyl-1-oxopentan-2-yl]carbamateHCID 104275—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12809805HCID 1280980538.8%

Reaction Conditions

Temperature10 °C

Reaction Steps

To diisopropylamine (7.7 g, 0.077 mol) in dry tetrahydrofuran (26 mL) cooled to -20 degrees C. under argon was added dropwise n-butyllithium in hexane (1.46M, 52.4 mL, 0.077 mol). The solution was stirred 15 min, the temperature lowered to -78 degrees C. and dry ethyl acetate (6.7 g, 0.077 mol) added dropwise while maintaining the temperature below -75 degrees C. The solution was stirred 10 min and a precooled (-78 degrees C.) tetrahydrofuran solution of Boc-L-leucinal (11 g, 0.051 mol) was added. After 30 min, 2M HCl (40 mL) was added and the mixture was slowly warmed to 10 degrees C. and extracted with ether (3×200 mL). The combined ethereal extract was washed with saturated sodium chloride and dried with magnesium sulfate and filtered. Evaporation of the filtrate in vacuo gave 14 g of crude product which was purified by flash chromatography (20% ethyl acetate in hexane) to give 6 g of desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05346887
Source datasetuspto-grants-1994_09
ORD IDord-d42294cb5db84db48308d1827ed963d7
Source noteuspto-grants-1994_09