HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23776Generated: October 29, 2026
Hydrochloric Acid → 2-Ethoxy-6-pentadecyl-benzyl alcohol
https://huagongshe.com/reaction/23776
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Ethyl 2-Ethoxy-6-pentadecylbenzoate | HCID 22574569 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | 2-Ethoxy-6-pentadecyl-benzyl alcohol | HCID 66701924 | — |
Reaction Steps
Ethyl 2-ethoxy-6-pentadecyl-benzoate (10.9 g, 27 mmol) was dissolved in dry tetrahydrofuran (60 mL). This solution was transferred to dry 250 mL three neck round bottom flask fitted with reflux condenser, mechanical stirrer and it was maintained under nitrogen atmosphere through out the reaction. To this lithium aluminum hydride (2.04 g, 54 mmol) was added slowly. Reaction was highly exothermic. After addition the solution was slowly brought to the reflux temperature and maintained at that temperature for about two hours and TLC was checked in hexane:EtOAc (8:2). After completion of reaction, excess lithium aluminium hydride was decomposed by drop-wise addition of ethylacetate (80 mL). To this 5 M HCl (100 mL) was added and organic layer was separated, dried over anhydrous sodium sulphate, concentrated under vacuum to give a light brownish solid. This was recrystallised from petroleum ether (40-60° C.) to give white solid. Yield: 8 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06852742B2 |
|---|
| Source dataset | uspto-grants-2005_02 |
|---|
| ORD ID | ord-80f67467bb55482e8f6dcd68548bf2ec |
|---|
| Source note | uspto-grants-2005_02 |
|---|