HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl 4-oxopiperidine-1-carboxylate → HCID 86686412, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl 4-oxopiperidine-1-carboxylate | HCID 643496 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | tert-Butyl alaninate hydrochloride | HCID 11275390 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 86686412 | HCID 86686412 | 97.5% |
Reaction Steps
To a solution of N-Cbz-4-piperidinone (3.497 g, 15.0 mmol) in dichloroethane (100 mL) was added L-alanine tert-butyl ester hydrochloride (2.731 g, 15.03 mmol) and sodium triacetoxyborohydride (6.47 g, 30.5 mmol). The mixture was stirred for 20 hours at room temperature, then quenched by the addition of saturated ammonium chloride (100 mL). The mixture was poured into ethyl acetate (500 mL), washed with water (2 times 100 mL), dried (MgSO4) and concentrated to yield the desired product (5.30 g, 97% yield). LC/MS: m/z 325.25 [M+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09321718B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-38ae7e601b8e48c7a7adddb1370eddf7 |
| Source note | uspto-grants-2016_04 |