HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253374Generated: November 1, 2026
Hydrochloric Acid → 3-(Trifluoromethyl)benzenepropanal
https://huagongshe.com/reaction/1253374
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Diisopropylaluminium hydride | HCID 21896610 | — |
| Reactant | Methyl 3-[3-(trifluoromethyl)phenyl]propanoate | HCID 53230361 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 3-(Trifluoromethyl)benzenepropanal | HCID 11298612 | 101.5% |
Reaction Steps
2.40 g of 3-(3-trifluoromethylphenyl)-propionic acid methyl ester synthesized in Step 1 was dissolved in 20 ml of dry dichloromethane. 13 ml of diisopropyl aluminum hydride solution (0.91 M) in hexane was dropped over 5 minutes at −78° C. under an argon atmosphere, and the mixture was stirred at the same temperature for 40 minutes. 50 ml of a saturated ammonium chloride aqueous solution was dropped, and then the mixture was stirred and the temperature was raised to room temperature. 20 ml of water and 5 ml of concentrated hydrochloric acid were added, and the resultant was separated into an aqueous layer and an organic layer. The aqueous layer was extracted with dichloromethane, and the extract was combined with the separated organic layer, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure to afford 2.12 g of the captioned compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08454978B2 |
|---|
| Source dataset | uspto-grants-2013_06 |
|---|
| ORD ID | ord-64c890373e31474e8e3db64fe1117611 |
|---|
| Source note | uspto-grants-2013_06 |
|---|