HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28067Generated: October 28, 2026
3-[1-(tert-butyloxycarbonyl)-L-prolylthio]-2-methylpropanoic acid → HCID 22810363, compound
https://huagongshe.com/reaction/28067
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-[1-(tert-butyloxycarbonyl)-L-prolylthio]-2-methylpropanoic acid | HCID 54552105 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Solvent | Anisole | HCID 7519 | — |
| Product | HCID 22810363 | HCID 22810363 | — |
Reaction Steps
3-[1-(tert-butyloxycarbonyl)-L-prolylthio]-2-methylpropanoic acid (2.3 g) is dissolved in a mixture of trifluoroacetic acid (15 ml) and anisole (1.1 g). After fifteen minutes at room temperature the mixture is concentrated to dryness in vacuo and the residue triturated with ether-hexane (1:1). The insoluble material is dried in vacuo, dissolved in dichloromethane (100 ml) and added dropwise to a stirred solution of 1-cyclohexyl-3-(2-morpholinoethyl) carbodiimide metho-p-toluene sulfonate (20 g) in 900 ml of dichloromethane under argon. The reaction mixture is stored at room temperature for three days and the dichloromethane is then removed in vacuo. The residue is dissolved in ethyl acetate and the solution is washed with 10% potassium biculfate, water, saturated sodium bicarbonate and water. The organic layer is dried and concentrated to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04225495 |
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| Source dataset | uspto-grants-1980_09 |
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| ORD ID | ord-bba19c084b9a448faece84517ff907c9 |
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| Source note | uspto-grants-1980_09 |
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