HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493035Generated: October 26, 2026
Hydrochloric Acid → (4-Propylphenyl)methanol
https://huagongshe.com/reaction/493035
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Methyl 4-propylbenzoate | HCID 12861010 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | (4-Propylphenyl)methanol | HCID 2760472 | 98.5% |
Reaction Steps
Dried tetrahydrofuran (50 ml) in which 10.4 g (58.4 mmol) of 4-n-propylbenzoic acid methyl ester synthesized in step (i) was dissolved was dropwise added to 50 ml of dried tetrahydrofuran containing suspension of lithium aluminium hydride (1.54 g: 40.5 mmol) at a temperature of not more than 10° C. with cooling with ice, and reaction was carried out at a room temperature overnight. After the completion of the reaction, an excess amount of lithium aluminium hydride was reacted with methanol with cooling with ice. Next water and an aqueous solution of hydrochloric acid were successively added to the reaction mixture, and the resultant was extracted with hexane. After the hexane phase was washed with water, hexane was removed from the hexane phase to give 8.63 g (57.5 mmol) of 4-n-propylbenzyl alcohol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07534547B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-a6779d30ec104bc38523bca87f1e820f |
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| Source note | uspto-grants-2009_05 |
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