HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1976535Generated: October 31, 2026
Pyridine → Methyl N-(oxomethylidene)phenylalaninate
https://huagongshe.com/reaction/1976535
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | Methyl L-phenylalaninate hydrochloride | HCID 75736 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl N-(oxomethylidene)phenylalaninate | HCID 1514293 | — |
Reaction Steps
A well-stirred cold mixture (0° C.) of phenylalanine methyl ester hydrochloride (200 mg), anhydrous dichloromethane (3 ml), and anhydrous pyridine (295 μl, 4 eq.) was stirred for 15 min. A 2M phosgene solution in toluene (455 μl, 0.98 eq.) was added over 30 sec. followed by stirring for 2 h at 0° C. The reaction mixture was poured into dichloromethane washed with cold IN hydrochloric acid then ice water. Each aqueous layer was back extracted once with dichloromethane. The combined organic layer was washed once with brine, dried over anhydrous magnesium sulfate and concentrated. Distillation under vacuum afforded methyl (S)-2-isocyanato-3-phenylpropanoate (125 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06228842B1 |
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| Source dataset | uspto-grants-2001_05 |
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| ORD ID | ord-6b54892e9b914fa993a77915ba2e691d |
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| Source note | uspto-grants-2001_05 |
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