HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Methyl (2S,3S)-3-t-butoxycarbonylamino-2-hydroxy-5-methylhexanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Diazomethane | HCID 9550 | — |
| Reactant | (2RS,3S)-3-tert-butyloxycarbonylamino-2-hydroxy-5-methylhexanoic acid | HCID 13848631 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Methyl (2S,3S)-3-t-butoxycarbonylamino-2-hydroxy-5-methylhexanoate | HCID 13420965 | — |
Reaction Steps
A solution of 1.00 g (3.8 mmole) of 3(S)-t-butoxycarbonylamino-2-hydroxy-5-methylhexanoic acid prepared by the method of R. L. Johnson [J. Med. Chem., 25, 605 (1982)] in 30 ml, of methanol was stirred, whilst cooling with ice, and then a diethyl ether solution of diazomethane was added and the mixture was stirred at room temperature for 1 hour. The solvent was then distilled off and the resulting solid was recrystallized from hexane to give 952 mg of the title product as colorless needles, melting at 84°-85° C.; [α]25 -10.2° (C=1.26, methanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04698329 |
| Source dataset | uspto-grants-1987_10 |
| ORD ID | ord-f1602008bb59499aa40402308358b05b |
| Source note | uspto-grants-1987_10 |