HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrabutylammonium borohydride → HCID 68157058, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrabutylammonium borohydride | HCID 169536 | — |
| Reactant | HCID 86668874 | HCID 86668874 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68157058 | HCID 68157058 | 82.1% |
Reaction Steps
Tetrabutylammonium borohydride (800 mg, 3.10 mmol) was added at RT to a solution of 3-o-tolylbenzo[b]thiophene-2-carbaldehyde (2.07 mmol) in THF (10 mL) and IMS (1 mL) and the mixture stirred at RT for 1 h. The reaction mixture was quenched by addition of MeOH and volatiles were removed under reduced pressure. The resulting residues was purified by column chromatography (Si—PCC, gradient 0-30% EtOAc in cyclohexane) affording the title compound as an oil (432 mg, 82% over 2 steps). LCMS (Method C): RT 3.74 min [M-OH]+ 237.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08653089B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-cba0b6f723a942f89638edc13dae137e |
| Source note | uspto-grants-2014_02 |