HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 262578Generated: October 26, 2026
4-Methylmorpholine → 1-[3-(triphenylmethylthio)-2-methylpropanoyl]-L-proline
https://huagongshe.com/reaction/262578
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | L-Proline | HCID 145742 | — |
| Reactant | 3-Triphenylmethylthio-2-methylpropanoic acid | HCID 21319154 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 1-[3-(triphenylmethylthio)-2-methylpropanoyl]-L-proline | HCID 54443075 | — |
Reaction Steps
3-Triphenylmethylthio-2-methylpropanoic acid (1.8 g.) and N,N'-carbonyldiimidazole (0.8 g.) are dissolved in tetrahydrofuran (10 ml.) with stirring at room temperature. After twenty minutes, the solution is added to a mixture of L-proline (0.6 g.) and N-methylmorpholine (1 g.) in dimethylacetamide (20 ml.). The resulting mixture is stirred overnight at room temperature, concentrated to dryness and the residue dissolved in a mixture of ethyl acetate and 10% aqueous potassium bisulfate. The organic layer is separated and dried and concentrated to dryness in vacuo to obtain 1-[3-(triphenylmethylthio)-2-methylpropanoyl]-L-proline. Rf :=0.4 (Silica gel, Benzene/acetic acid 3:1), Rf 1.0 (Silica gel, Methyl-ethylketone/acetic acid/pyridine/water 14:1:2:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04154840 |
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| Source dataset | uspto-grants-1979_05 |
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| ORD ID | ord-0dcaf26feb994f5db5c9cabb3078a35f |
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| Source note | uspto-grants-1979_05 |
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