HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Bicarbonate → 1-(7-Hydroxymethyl-benzofuran-5-yl)-ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 21220947 | HCID 21220947 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(7-Hydroxymethyl-benzofuran-5-yl)-ethanone | HCID 21220889 | 57.8% |
Reaction Steps
A solution of 5-acetyl-benzofuran-7-carbaldehyde (471 mg) in dry toluene (40 ml) was treated with sodium triacetoxyborohydride (1.12 ml) and heated at reflux for 5.5 h. The reaction mixture was poured into 8% sodium bicarbonate (40 ml) and the phases were separated. The aqueous phase was extracted with ethyl acetate (40 ml), the combined organic phases were dried, filtered, and the filtrate evaporated in vacuo to give a yellow gum. Purification by FCC eluted with hexane:ethyl acetate (2:1→1:1) gave the title compound as a pale yellow oil (275 mg) which slowly solidified.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05935972 |
| Source dataset | uspto-grants-1999_08 |
| ORD ID | ord-708bb31745db4974a2a603adb9bad6f2 |
| Source note | uspto-grants-1999_08 |