HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280113Generated: October 28, 2026
HCID 23321921, compound → HCID 12801697, compound
https://huagongshe.com/reaction/280113
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 23321921 | HCID 23321921 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Solvent | Anisole | HCID 7519 | — |
| Product | HCID 12801697 | HCID 12801697 | 45.1% |
Reaction Steps
Crude N-(3-acetylthio-2-methylpropanoyl)-N-furfurylglycine tert-butyl ester (14.6 g, 0.0407 mol) was dissolved in a mixture of anisole (20 ml) and trifluoroacetic acid (65 ml). The resulting solution was stirred at room temperature for two hours. The solvent was evaporated in vacuo and the residue was distributed between ethyl acetate and saturated aqueous sodium bicarbonate. The aqueous bicarbonate extract was washed twice with ethyl acetate and then acidified cautiously with concentrated hydrochloric acid to pH 4-5. The product was extracted several times into chloroform and the chloroform was washed twice with water. The organic phase was dried over magnesium sulfate, filtered and evaporated to give crude product as a pale yellow oil which was purified by HPLC using the following solvent system: ethyl acetate/n-hexane/acetic acid (40:60:1) to give pure product as a colorless oil (5.5 g, 44.7%). The product was purified by its DCHA salt which was prepared in ether, m.p. 140°-141° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04588734 |
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| Source dataset | uspto-grants-1986_05 |
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| ORD ID | ord-13e700f23b244d0d8da75155375d23b5 |
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| Source note | uspto-grants-1986_05 |
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