HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → [3-(2-Methanesulphinyl-ethoxy)-phenyl]-methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-(2-Methanesulphinyl-ethoxy)-benzaldehyde | HCID 59259179 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | [3-(2-Methanesulphinyl-ethoxy)-phenyl]-methanol | HCID 59259025 | — |
Reaction Steps
To a solution of 1.1 g (5.18 mmol) 3-(2-methanesulphinyl-ethoxy)-benzaldehyde in 20 ml ethanol (anhydrous) is added NaBH4 (0.215 g, 5.7 mmol). The reaction mixture is stirred at room temperature for 0.5 h. Then it is poured onto water and extracted with ethyl acetate. The combined organic layers are washed with water and brine, dried over MgSO4, filtered and concentrated in vacuo to afford the title compound as a colorless oil that is of sufficient purity for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08569317B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-5650063affcf4468b9a1d868358aa9ac |
| Source note | uspto-grants-2013_10 |