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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1266512Generated: November 2, 2026

Hydrochloric Acid → HCID 22708149, compound

https://huagongshe.com/reaction/1266512

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFurfuralHCID 7362—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantTert-butyl 2-(4-(2-aminoethyl)phenylthio)-2-methylpropanoateHCID 11623510—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 22708149HCID 2270814947.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

4.0 g of 1,1-dimethylethyl 2-[[4-(2-aminoethyl)phenyl]thio]-2-methyl-propanoate [(P. J. Brown et al., J. Med. Chem. 42, 3785-88 (1999)] are dissolved in 100 ml of methanol and treated with 2.6 g of furfural. 9.3 ml of glacial acetic acid are added and the mixture is boiled briefly (10 min). The mixture is then cooled to 0° C., and 4.25 g of sodium cyanoborohydride are added a little at a time. The mixture is then stirred at room temperature overnight. 1 N HCl is added until the mixture is acidic, and the mixture is stirred for 30 min. The mixture is concentrated slightly and made basic using sat. NaHCO3 solution. The mixture is then extracted twice with ethyl acetate and the extracts are washed (sat. NaCl solution) and dried and concentrated. Chromatographic purification (dichloromethane/methanol 15+1) gives 2.4 g of the title compound as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06548538B2
Source datasetuspto-grants-2003_04
ORD IDord-ba61f9b29c6f4acc90ff22468a7be0e9
Source noteuspto-grants-2003_04