HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dibenzo(b,d)furan-2-carboxaldehyde → 2-Dibenzofuranmethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dibenzo(b,d)furan-2-carboxaldehyde | HCID 220843 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Dibenzofuranmethanol | HCID 290846 | — |
Reaction Steps
To a solution of dibenzo[b,d]furan-2-carbaldehyde (191 mg, 973 μmol) in THF (10 mL) in a 50 mL round-bottomed flask equipped with a magnetic stirrer was added NaBH4 (37 mg, 0.978 mmol) and the mixture was stirred for 2 h at RT and quenched by adding 10 mL of a 1 N aq. HCl solution. The reaction mixture was stirred at RT for 20 min and extracted with CH2Cl2 (2×50 mL). The organic phase was washed with water (10 mL), brine (10 mL), dried over Na2SO4, filtered and concentrated at 40° C. under vacuum to afford dibenzo[b,d]furan-2-ylmethanol CCH 34116 as an off-white solid (192 mg, 100% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08772316B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-b27249f368fd40b18b28f1140564a95c |
| Source note | uspto-grants-2014_07 |