HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → tert-Butyl 6-cyano-4-hydroxy-spiro[chroman-2,4'-piperidine]-1'-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Tert-butyl 6-cyano-4-oxo-3,4-dihydrospiro[1-benzopyran-2,4'-piperidine]-1'-carboxylate | HCID 66649586 | — |
| Solvent | Tetrahydrofuran ethanol | HCID 21873804 | — |
| Product | tert-Butyl 6-cyano-4-hydroxy-spiro[chroman-2,4'-piperidine]-1'-carboxylate | HCID 66649142 | — |
Reaction Steps
To a solution of 15 g of tert-butyl 6-cyano-4-oxospiro[chroman-2,4′-piperidine]-1′-carboxylate in 250 mL of EtOH-THF(1:4) at 0° C. was added NaBH4 portionwise, and the reaction mixture was allowed to warm up to rt. After stirring for 1 h, NH4Cl aqueous was added to the reaction mixture and the aqueous mixture was extracted with AcOEt twice. The combined organic layers were washed with brine, dried over Na2SO4, filtered, and concentrated in reduced pressure to give the intended compound as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08138197B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-e7d84f57c9d248509eddb5e8ef418e95 |
| Source note | uspto-grants-2012_03 |