HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248271Generated: October 30, 2026
Hydrochloric Acid → Methyl 2-amino-3-(phenylsulfanyl)propanoate
https://huagongshe.com/reaction/1248271
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl 2-azido-3-(phenylsulfanyl)propanoate | HCID 13192751 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Rhenium | HCID 23947 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 2-amino-3-(phenylsulfanyl)propanoate | HCID 13192752 | 80.1% |
Reaction Steps
0.91 gram (3.84 mmoles) of the 2-azido-3-phenylmercapto-propionic acid methyl ester obtained in Example 2 in 8 ml of methanol was treated with 0.28 gram (7.68 mmoles) of hydrogen chloride, 1 mole % of rhenium VII sulfide based on the azido compound employed was added and the mixture hydrogenated in an autoclave at a hydrogen pressure of 60 bar at 25° C. for 3.5 hours. After the end of the reaction the catalyst was filtered off with suction, the solvent remained under reduced pressure and the residue treated with 20 ml of acetone. After addition of 20 ml of diethyl ether for complete precipitation, the precipitate was filtered off with suction, then washed with diethyl ether and dried at 40° C. for 12 hours under reduced pressure. There were obtained 0.65 gram (68% of theory) of 2-amino-3-phenylmercapto-propionic acid methyl ester.HCl with a melting point of 123° to 125° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04523012 |
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| Source dataset | uspto-grants-1985_06 |
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| ORD ID | ord-fa846467bfa343a590d7b51f65cd936e |
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| Source note | uspto-grants-1985_06 |
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