HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781172Generated: October 31, 2026
4-Phenoxybenzaldehyde → HCID 19069360, compound
https://huagongshe.com/reaction/1781172
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Phenoxybenzaldehyde | HCID 66139 | — |
| Reactant | Cyclopropanemethanamine | HCID 75646 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 19069360 | HCID 19069360 | 78.4% |
Reaction Steps
4-Phenoxybenzaldehyde (3.0 g, 15.1 mmol) and cyclopropylmethylamine (1.1 g, 15.1 mmol) were dissolved in methanol (85 mL) under a nitrogen at room temperature. Sodium cyanoborohydride (0.95 g, 15.1 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 3.0 g (78%) of the title compound as a colorless oil. 1H NMR (CDCl3, 300 MHz) δ 0.08-0.15 (m, 2H), 0.45-0.55 (m, 2H), 0.93-1.05 (m, 1H), 1.45 (br s, 1H), 2.50 (d, J=7.5 Hz, 2H), 3.78 (s, 2H), 6.95-7.03 (m, 4H) 7.05-7.13 (m, 1H), 7.25-7.38 (m, 4H). MS (DCl/NH3) m/e 254 (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-f2de4ea21ddf47a4ae1d1a025ccb0681 |
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| Source note | uspto-grants-1997_05 |
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