HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → (2-Benzyloxy-5-methoxymethoxyphenyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-Benzyloxy-5-methoxymethoxybenzaldehyde | HCID 17861251 | — |
| Solvent | Water | HCID 962 | — |
| Product | (2-Benzyloxy-5-methoxymethoxyphenyl)methanol | HCID 17861294 | 99.8% |
Reaction Steps
To a mixture of 2-benzyloxy-5-methoxymethoxybenzaldehyde (10.03 g), ethanol (50 mL) and tetrahydrofuran (100 mL) was added sodium tetrahydroborate (1.43 g) under ice-cooling, and the mixture was stirred at room temperature for 1 hr. To the reaction mixture was added water and the mixture was extracted with ethyl acetate. The organic layer was washed successively with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated to give (2-benzyloxy-5-methoxymethoxyphenyl)methanol as a colorless oil (10.08 g, 97%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07238716B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-216d3aabc43a42bf84ce93a06b49a3db |
| Source note | uspto-grants-2007_07 |