HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1041233Generated: October 31, 2026
Tetrahydrofuran → (4-Methoxy-1,2-phenylene)dimethanol
https://huagongshe.com/reaction/1041233
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Lithium aluminum hydride | HCID 28112 | — |
| Reactant | Dimethyl 4-methoxyphthalate | HCID 736307 | — |
| Product | (4-Methoxy-1,2-phenylene)dimethanol | HCID 12577527 | 97% |
Reaction Steps
To a stirred suspension of Lithium tetrahydroaluminate (16.6 g, 0.436 mol) in Tetrahydrofuran (300 mL, 4 mol) at 0° C. under nitrogen was added dropwise a solution of 4-Methoxy-phthalic acid dimethyl ester (24.46 g, 0.1091 mol) in Tetrahydrofuran (100 mL, 1 mol). The reaction was stirred at 0° C. for 1 h then warmed to room temperature overnight. HPLC indicated no starting material present. Reaction was recooled at 0° C. and quenched with addition of water (125 mL) carefully dropwise, 1 N NaOH (100 mL) and water (125 mL). Evolution of gas was observed upon initial quenching with water. A white solid precipitated out of solution (aluminum salts). Following complete quenching of the reaction mixture, the aluminum salts were removed by filtration. The filtrate was diluted with ethyl acetate, washed with water, dried over magnesium sulfate, filtered and concentrated in vacuo to provide 17.80 grams (97%) of (2-Hydroxymethyl-4-methoxy-phenyl)-methanol as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08552186B2 |
|---|
| Source dataset | uspto-grants-2013_10 |
|---|
| ORD ID | ord-0c1e27afd2294d91ad06c1e25310cd46 |
|---|
| Source note | uspto-grants-2013_10 |
|---|