HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 67247455, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 13419512 | HCID 13419512 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 67247455 | HCID 67247455 | — |
Reaction Steps
To a mixture of 1-(1-bromo-2-naphthyl)ethanone (0.488 g, 1.96 mmol) in methanol (10 mL) was added sodium tetrahydroborate (0.0741 g, 1.96 mmol). The reaction was stirred at room temperature for 30 minutes, quenched with water, extracted with ethyl acetate. The combined organic layers were washed with brine, dried over magnesium sulfate, and concentrated to dryness under reduced pressure. The residue was used directly in next step (467 mg, 94%). LCMS calculated for C12H10Br(M−OH)+: m/z=233.0; found: 233.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08680108B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-a6e6a892f7614ae18657c36d1876f738 |
| Source note | uspto-grants-2014_03 |