HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1112400Generated: October 25, 2026
Hydrochloric Acid → 4-(Decyloxy)benzaldehyde
https://huagongshe.com/reaction/1112400
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 4-(Decyloxy)benzoic acid | HCID 138527 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(Decyloxy)benzaldehyde | HCID 141068 | — |
Reaction Steps
To a mixture of 27.8 g (0.1 mole) of 4-(decyloxy)benzoic acid in 500 ml of tetrahydrofuran cooled to 0° C. is slowly added 16.2 g (0.1 mole) of N,N'-carbonyldiimidazole. The mixture is heated to reflux for 1 hour then cooled to -20° C. To the cooled mixture is added 1.9 g (0.05 mole) of lithium aluminum hydride and stirring is continued at -20° C. for 1 hour. To the reaction mixture is slowly added 100 ml of 5% aqueous hydrochloric acid followed by the addition of ether. The ether layer is separated and washed with 5% aqueous hydrochloric acid, water, and 5% aqueous sodium bicarbonate then dried over sodium sulfate, filtered and evaporated to dryness to give 4-(decyloxy)benzaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04122191 |
|---|
| Source dataset | uspto-grants-1978_10 |
|---|
| ORD ID | ord-8d30fda8223a40b0ba8a6b0097fd026d |
|---|
| Source note | uspto-grants-1978_10 |
|---|