HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium sulfate decahydrate → 3,5-Bis(methoxymethoxy)benzylalcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium sulfate decahydrate | HCID 62649 | — |
| Reactant | Methyl 3,5-bis(methoxymethoxy)benzoate | HCID 10106435 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3,5-Bis(methoxymethoxy)benzylalcohol | HCID 10443751 | 94% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
The above-obtained 3,5-bis(methoxymethoxy)benzoic acid methyl ester (9.1 g, 36 mmol) was dissolved in diethylether (50 mL) and cooled to 0° C. To the obtained solution, lithium aluminum hydride (2.0 g, 54 mmol) was slowly added followed by stirring at 0° C. for 2 hours. The reaction mixture was further added with sodium sulfate decahydrate (40 g), and was stirred for another 1 hour. The reaction mixture was filtered, and the obtained filtrate was concentrated under reduced pressure to obtain 3,5-bis(methoxymethoxy)phenylmethanol (7.6 g, 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07781485B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-e1c7a66c8d4143b2a4a441cb283b90f1 |
| Source note | uspto-grants-2010_08 |