HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781175Generated: October 30, 2026
4-Phenoxybenzaldehyde → HCID 54419610, compound
https://huagongshe.com/reaction/1781175
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Phenoxybenzaldehyde | HCID 66139 | — |
| Reactant | (+)-1-(1-Naphthyl)ethylamine | HCID 2724264 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 54419610 | HCID 54419610 | 77% |
Reaction Steps
4-Phenoxybenzaldehyde (2.34 g, 11.8 mmol) and (2R)-2-(1-naphthyl)eth-2-ylamine (2.02 g, 11.8 mmol) were dissolved in methanol (39 mL) under a nitrogen at room temperature. Sodium cyanoborohydride (742 mg, 11.8 mmol) was added, and stirring was continued for 48 hours. The solvent was evaporated and the residue was suspended in ether, washed with brine, and dried over Na2SO4. The ether was evaporated, and the crude product was chromatographed on silica gel eluting with 3% methanol in methylene chloride to provide 3.21 g (77%) of the title compound as a colorless oil. 1H NMR (CDCl3, 300 MHz), δ 1.52 (d, J=6 Hz, 3H), 1.64 (s, 1H), 3.7 (dd, J=13.5 Hz, 7.5 Hz, 2H), 4.7 (q, J=7.5 Hz, 1H), 6.95 (m, 4H), 7.08 (m, 1H), 7.3 (m, 4H), 7.5 (m, 3H), 7.75 (m, 2H), 7.9 (m, 1H), 8.15 (m, 1H). MS (DCl/NH3) m/e 354 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05631401 |
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| Source dataset | uspto-grants-1997_05 |
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| ORD ID | ord-16dc2ea20903429ca8b50e928cc61352 |
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| Source note | uspto-grants-1997_05 |
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