HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → tert-butyl((2S)-3-hydroxyhexan-2-yl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | (S)-tert-butyl(3-oxohexan-2-yl)carbamate | HCID 75406864 | — |
| Solvent | Isopropanol methanol | HCID 21255859 | — |
| Product | tert-butyl((2S)-3-hydroxyhexan-2-yl)carbamate | HCID 87514848 | 96.2% |
Reaction Steps
Sodium borohydride (3.7 g) was added in divided portions to a methanol/isopropanol (30 ml/30 ml) solution containing (S)-tert-butyl(3-oxohexan-2-yl)carbamate (17.5 g) at room temperature, followed by stirring for 1 hour. The solvent was distilled away under reduced pressure, and water was added, followed by extraction with ethyl acetate. The obtained organic layer was washed with saturated saline and dried over anhydrous sodium sulfate, the solvent was distilled away under reduced pressure, and a white solid of tert-butyl((2S)-3-hydroxyhexan-2-yl)carbamate (17 g) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08895585B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-372ca76a0f464f6e9fda63163dd732f4 |
| Source note | uspto-grants-2014_11 |