HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353178Generated: October 29, 2026
Hydrochloric Acid → HCID 22708149, compound
https://huagongshe.com/reaction/353178
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Furfural | HCID 7362 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | Tert-butyl 2-(4-(2-aminoethyl)phenylthio)-2-methylpropanoate | HCID 11623510 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 22708149 | HCID 22708149 | 47.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06750236B2 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-b9567585f4ee466f84eaa5bfb7dd068e |
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| Source note | uspto-grants-2004_06 |
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