HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 67515018, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 67508114 | HCID 67508114 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67515018 | HCID 67515018 | 70% |
Reaction Steps
Ethyl 5-(benzyloxycarbonylamino)-5-methyl-3-oxohexanoate (3.49, 10.9 mmol) was dissolved in ethanol (100 ml). Sodium borohydride (1.64 g, 43.4 mmol) was added to the mixture, and the reaction mixture was stirred for 3 hours at room temperature. The reaction was quenched with 1 N HCl, and the mixture was stirred for 1 hour. The mixture was extracted with ethylacetate, and the combined organic layers were dried over sodium sulfate, filtered, and purified by column chromatography (0 to 4% methanol on dichloromethane) to give 2.14 g (70%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09248117B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-96d0914212db4294b2c2a4e23e4fd24a |
| Source note | uspto-grants-2016_02 |