HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 59342433, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 4-(1-Chloro-2-oxo-propylidene)piperidine-1-carboxylic acid tert-butyl ester | HCID 58804090 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59342433 | HCID 59342433 | 72.2% |
Reaction Steps
A solution of 55 (1.24 g, 4.53 mmol) in ethanol (25 mL) was treated with sodium borohydride (102 mg, 2.72 mmol) at 25° C. After 1 h, the reaction mixture was concentrated in vacuo, diluted with ethyl acetate (40 mL), carefully treated with 5% aqueous hydrochloric acid (1×25 mL), the layers separated, and dried (MgSO4). The resulting solution was concentrated in vacuo to afford 56 (902.1 mg, 72%) as a colorless residue that was used without further purification. MS 298 (M+Na).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07732612B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-bbfe50f7dc384634a1d9096f12d01bd6 |
| Source note | uspto-grants-2010_06 |