HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diazomethane → Methyl (2S,3S)-3-t-butoxycarbonylamino-2-hydroxy-5-methylhexanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diazomethane | HCID 9550 | — |
| Reactant | N-Boc-(2S,3S)-2-hydroxy-3-amino-5-methylhexanoic acid | HCID 2762291 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl (2S,3S)-3-t-butoxycarbonylamino-2-hydroxy-5-methylhexanoate | HCID 13420965 | — |
Reaction Steps
To a solution of 1.00 g (3.8 mmole) of (2S,3S)-3-(t-butoxycarbonyl)amino-2-hydroxy-5-methylhexaneoic acid prepared according to the method of R. L. Johnson [J. Med. Chem., 25, 605 (1982)] in 30 ml. of methanol was added, with stirring and ice-cooling, an ethereal solution of diazomethane. The mixture was stirred at room temperature for 1 hour. The solvent was removed by distillation, and the solid thus obtained was recrystallized from hexane, to afford 952 mg. of colourless needles, melting at 84°-85° C.; [α]22 -10.2° (C=1.26, methanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04548926 |
| Source dataset | uspto-grants-1985_10 |
| ORD ID | ord-be12f9d54cb544d585073c170e84b1a0 |
| Source note | uspto-grants-1985_10 |