HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 11461534, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | tert-Butyl 4-(4-chlorobenzoyl)piperidine-1-carboxylate | HCID 10519988 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 11461534 | HCID 11461534 | 94.8% |
Reaction Steps
tert-Butyl 4-(4-chlorobenzoyl)piperidine-1-carboxylate (3.63 g, 11.2 mmol) was dissolved in ethanol (100 mL) then sodium tetrahydroborate (424 mg, 112 mmol) was added to this solution. The reaction mixture was stirred at room temperature for 3 h. LC-MS analysis of the reaction mixture showed no more starting material. The crude reaction mixture was concentrated and the residue was diluted with EtOAc (100 mL) and washed with water (2×50 mL) and brine (50 mL). The organic layer was dried over Na2SO4, filtered and concentrated to yield tert-butyl 4-((4-chlorophenyl)(hydroxy)methyl)piperidine-1-carboxylate (3.46 g, 94%), which was used in the next step directly. m/z: 326 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09328091B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-dde20869caa04610881206ff1d16c836 |
| Source note | uspto-grants-2016_05 |