HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855202Generated: October 28, 2026
Hydrochloric Acid → HCID 17078919, compound
https://huagongshe.com/reaction/855202
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 3-Phenylpropylamine | HCID 16259 | — |
| Reactant | 4-tert-Butylbenzaldehyde | HCID 70324 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 17078919 | HCID 17078919 | — |
Reaction Steps
0.38 ml of 4-tert-butylbenzaldehyde (2.25 mmol) and 0.213 ml of 3-phenylpropylamine (1.5 mmol) were dissolved in 5 ml methanol at rt, and after stirring for 30 min at rt, were refluxed for 2 h. After cooling down to rt, 85 mg (2.25 mmol) of sodium borohydride were added and after 10 min stirring at rt, the reaction mixture was then refluxed for 3 h. After cooling down to rt, the reaction mixture was treated with 0.15 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, 558 mg of a light brown oil, was not further purified and used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07259183B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-484cf5d983b74e6eaca81474d3267762 |
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| Source note | uspto-grants-2007_08 |
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