HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → Benzenemethanol, 5-bromo-2-(methoxymethoxy)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-Bromo-2-(methoxymethoxy)benzaldehyde | HCID 19701626 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Benzenemethanol, 5-bromo-2-(methoxymethoxy)- | HCID 54142346 | 100% |
Reaction Steps
To a solution of 5-bromo-2-methoxymethoxybenzaldehyde (5.00 g) in methanol (50 ml) was added, at 0° C., sodium borohydride (0.46 g). The mixture was stirred for 30 minutes at the same temperature, which was then concentrated. To the concentrate was added ethyl acetate, and the mixture was washed with an aqueous solution of potassium hydrogensulfate and a saturated aqueous saline solution, successively. The organic layer was dried (anhydrous magnesium sulfate), which was then concentrated to leave 5-bromo-2-methoxymethoxybenzyl alcohol (5.04 g) as a pale yellow oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05716971 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-0a810795ea7145fd8dc67a46d3fa7d98 |
| Source note | uspto-grants-1998_02 |