HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488177Generated: October 30, 2026
4-Hydroxybenzaldehyde → HCID 22860522, compound
https://huagongshe.com/reaction/488177
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | (αR)-4-Methyl-α-phenylbenzeneethanamine | HCID 10138221 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22860522 | HCID 22860522 | 64.5% |
Reaction Steps
21.13 g (0.1 mole) of (R)-(-)-α-phenyl-β-p-tolylethylamine (optical purity: 100%) and 12.82 g (0.105 mole) of p-hydroxybenzaldehyde were dissolved in 750 ml of ethyl alcohol. The reaction solution thus obtained was stirred at room temperature for 3 hours, and then stirred under reflux for 1 hour. Thereafter, the reaction solution was admixed at room temperature with 1.89 g (0.05 mole) of sodium borohydride, stirred for 3 hours, and then stirred under reflux for 1 hour. The reaction mixture was admixed with 75 ml of a 10% hydrochloric acid, and then concentrated under reduced pressure to give a crude (R)-(+)-N-p-hydroxybenzyl-α-phenyl-β-p-tolylethylamine·HCl salt, which was thereafter neutralized with an aqueous sodium hydroxide solution. The resultant solution was concentrated under reduced pressure to obtain the crystals, which were then recrystallized from ethyl alcohol, so that 20.47 g of (R)-(+)-N-p-hydroxybenzyl-α-phenyl-β-p-tolylethylamine were obtained as colorless crystals. Yield: 64.5%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05298660 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-d829edc27d1f44b6a001e63fc7df375e |
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| Source note | uspto-grants-1994_03 |
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