HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855214Generated: October 29, 2026
Hydrochloric Acid → HCID 68576716, compound
https://huagongshe.com/reaction/855214
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-tert-Butylbenzaldehyde | HCID 70324 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2-(4-Chloro-3-trifluoromethyl-phenyl)-ethylamine hydrochloride | HCID 68560752 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 68576716 | HCID 68576716 | 88% |
Reaction Steps
1.54 ml of 4-tert-butylbenzaldehyde (9.23 mmol), 1.6 g of 2-(4-chloro-3-trifluoromethyl -phenyl)-ethylamine hydrochloride (6.15 mmol) and 850 mg of potassium carbonate (6.15 mmol) were suspended in 18 ml methanol at rt, and after stirring for 30 min at rt, were refluxed for 2 h. After cooling down to rt, 349 mg (9.23 mmol) of sodium borohydride were added and after stirring for 5 min at rt, the reaction mixture was refluxed for 2.5 h. After cooling down to rt, the reaction mixture was treated with 1.2 ml 1 N HCl and concentrated in vacuo. The residue was diluted with water/EtOAc. After separation of the organic phase, the aqueous phase was extracted with EtOAc and the combined organic phases were washed with brine, dried with magnesium sulfate, filtered off and concentrated in vacuo. The residue was purified by column chromatography (40 g silica gel; EtOAc/heptane 1:2) to give 2.01 g light yellow oil (88%). MS (ISP) 370.2 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07259183B2 |
|---|
| Source dataset | uspto-grants-2007_08 |
|---|
| ORD ID | ord-8d23376a668b48a3be9008a3caf3d06a |
|---|
| Source note | uspto-grants-2007_08 |
|---|