HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 86686410, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | tert-Butyl 2-oxopiperidine-1-carboxylate | HCID 7577838 | — |
| Reactant | HCID 86686411 | HCID 86686411 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 86686410 | HCID 86686410 | 100.3% |
Reaction Steps
To a solution of N-Boc-piperidinone (2.00 g, 10.0 mmol) in dichloroethane (25 mL) was added α,α-dimethylglycine cyclopentyl ester tosylate (3.97 g, 11.6 mmol) and sodium triacetoxyborohydride (4.248 g, 20.0 mmol). The mixture was stirred at room temperature for 22 hours then poured into ethyl acetate (300 mL). The organic layer was washed with water (3 times 100 mL), dried (MgSO4) and concentrated to yield the desired product (3.556 g, 84% yield) which was carried forward without further purification. LC/MS: m/z 355.25 [M+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09321718B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-408d6ddca724439baed1e9817863e8fd |
| Source note | uspto-grants-2016_04 |