HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → (S)-methyl 4-(tert-butoxycarbonylamino)-5-hydroxypentanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | (S)-2-((tert-butoxycarbonyl)amino)-5-methoxy-5-oxopentanoic acid | HCID 7018756 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-methyl 4-(tert-butoxycarbonylamino)-5-hydroxypentanoate | HCID 11107667 | 49% |
Reaction Steps
To a solution (S)-2-(tert-butoxycarbonylamino)-5-methoxy-5-oxopentanoic acid (26.1 g, 0.1 mol) in THF (500 mL), BH3.Me2S (80 mL, 0.8 mmol) was added dropwise at −78° C., then stirred at rt for 3 hrs. The reaction was stopped by careful addition of methanol. After evaporation and three distillations of methanol, the residue was dissolved in EtOAc, washed with 1 M NaHCO3, and brine. (S)-methyl 4-(tert-butoxycarbonylamino)-5-hydroxypentanoate (12 g, yield 49%) was obtained as an oil that was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08487108B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-7c10b6e8df794ab78bcc16b9d584b0d9 |
| Source note | uspto-grants-2013_07 |