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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384458Generated: October 31, 2026

Hydrochloric Acid → HCID 9816448, compound

https://huagongshe.com/reaction/1384458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylsilaneHCID 12052—
ReactantHCID 11056128HCID 11056128—
SolventFormic AcidHCID 284—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 9816448HCID 981644813%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of methyl N-[(S)-1-(4-methoxyphenyl)ethyl)-(S)-3-amino-3-(3-pyridyl)propanoate (57.35 g, 0.148 mol) and triethylsilane (25.81 g, 0.222 mol) in formic acid (120 mL) was heated to 90° C. (oil-bath) while stirring. The initial suspension became a clear solution after 5 minutes at 90° C. Heating and stirring was continued for 2 h. The reaction mixture was cooled to room temperature and the solvent was removed under reduced pressure at 50° C. to give a residual oil. The residual oil was dissolved in ethyl acetate (300 mL) and methanol (100 mL). The solution was filtered. The filtrate was treated slowly with 9.8 M HCl in methanol (30.2 mL, 0.296 mol) with stirring. The resulting solution was diluted with ethyl acetate (200 mL) and heated on a steam-bath to remove excess methanol until the solution became cloudy. The mixture was then stirred at room temperature overnight and the solid product crystallized from the solution. Ethyl acetate (150 mL) was added to the suspension and the mixture was stirred for another 2 h. The solid was collected by filtration and washed with 200 mL of ethyl acetate, then dried in vacu for 1 h. The desired product was obtained as a white powder (27.05 g, 72% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06258956B1
Source datasetuspto-grants-2001_07
ORD IDord-e2d23c4c6f104ebda84b05bf0815073f
Source noteuspto-grants-2001_07