HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 3-(4-Hydroxyphenyl)propanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 3-(4-acetylphenyl) propionic acid | HCID 312883 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(4-Hydroxyphenyl)propanol | HCID 82452 | 65% |
Reaction Steps
To 3.82 g (17.36 mmoles) of methyl ester of 3-(4-acetylphenyl) propionic acid were added 100 ml of dry tetrahydrofurane. To this solution were slowly added 1.80 g (47.43 mmoles) of lithium aluminium hydride (LiAlH4). The reaction mixture was refluxed in an argon atmosphere for 4 hours. At the end of the reaction, water was carefully added, extraction was performed three times with diethyl ether and the result was vacuum dried over anhydrous sodium sulphate, giving 1.70 g (65% yield) of 3-(4-hydroxyphenyl)-1-propanol. Crystallisation in methanol gave a white crystalline solid m,.p.=52-53° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06818780B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-394c5c7dc81d4cbbb7584b9649f69286 |
| Source note | uspto-grants-2004_11 |