HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → BENZYL 2-HYDROXYMETHYLBENZOATE
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Benzyl 4-formylbenzoate | HCID 11528845 | — |
| Solvent | Water | HCID 962 | — |
| Product | BENZYL 2-HYDROXYMETHYLBENZOATE | HCID 11356918 | — |
Reaction Steps
10.3 g (43 mmol) of benzyl 4-formylbenzoate, 50 ml of THF and 50 ml of methyl alcohol are introduced into a round-bottomed flask. While cooling in an icebath, 820 mg (21.5 mmol) of sodium borohydride are added in small portions and the mixture is stirred at room temperature for two hours. The reaction medium is poured into water, the mixture is extracted with ethyl ether and the organic phase is separated after settling has taken place, dried over magnesium sulphate and evaporated. 10.4 g (100%) of the expected product, melting point 55°-56° C., are collected.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05439925 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-d56683a6fac74f23abc6f32b1e6fcff9 |
| Source note | uspto-grants-1995_08 |