HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243111Generated: November 1, 2026
Thiophenol → Alanine, N-ethyl-, methyl ester (7CI)
https://huagongshe.com/reaction/2243111
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 68548246 | HCID 68548246 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Alanine, N-ethyl-, methyl ester (7CI) | HCID 53407612 | 31.1% |
Reaction Steps
Methyl 2-[ethyl(2-nitrobenzenesulfonyl)amino]propionate (8.07 g; 25.5 mmol) is dissolved in 250 ml of acetonitrile, and thiophenol (1.12 eq.; 28.7 mmol; 2.93 ml) and K2CO3 (3.25 eq.; 82.9 mmol; 11.45 g) are then added. The reaction medium is stirred overnight at room temperature. The crude product is evaporated to dryness and then taken up in ether. The organic phase is acidified with 1N hydrochloric acid and then washed with water. The aqueous phases are combined and then washed with ether and basified with potassium carbonate. The basic aqueous phase is extracted with ether three times. The three ether phases are washed with water and then with saturated aqueous sodium chloride solution, dried over sodium sulfate and evaporated to dryness to give 1.04 g of the expected product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07674803B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-32c7055a59564f21b6b042cdd5aa4451 |
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| Source note | uspto-grants-2010_03 |
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