HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545940Generated: October 30, 2026
4-Phenoxybenzaldehyde → HCID 59263537, compound
https://huagongshe.com/reaction/545940
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Phenoxybenzaldehyde | HCID 66139 | — |
| Reactant | Cyclopropanemethanamine | HCID 75646 | — |
| Reactant | Triacetoxyborohydride | HCID 2724942 | — |
| Reactant | HCID 86609017 | HCID 86609017 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59263537 | HCID 59263537 | 63.7% |
Reaction Steps
To a solution of 3-(2′-oxospiro[furo[2,3-f][1,3]benzodioxole-7,3′-indol]-1′(2′H)-yl)propanal (0.07 g, 0.20 mmol) in THF (5.00 mL) was added (aminomethyl)cyclopropane (0.30 mmol) and MP-triacetoxyborohydride (0.26 g, 0.60 mmol). After overnight shaking, the polymer-bound 4-phenyloxybenzaldehyde (0.25 g, 0.18 mmol) was added. After another overnight shaking, the mixture was diluted with ether (10.0 mL) and filtered. The filtrate was concentrated in vacuo to dryness. The residue was recrystallized to give the title compound (0.05 g) in 62% yield as a white solid: 1H NMR (300 MHz, CDCl3) δ 7.32-6.92 (m, 4H), 6.49 (s, 1H), 6.12 (s, 1H), 5.83 (m, 2H), 4.86 (m, 1H), 4.64 (m, 1H), 3.97-3.77 (m, 2H), 2.87-2.80 (m, 2H), 2.66-2.56 (m, 2H), 1.02-0.94 (m, 1H), 0.56-0.47 (m, 2H), 0.25-0.18 (m, 2H); MS (ES+) m/z 393.3 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07935721B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-5716b650fd5644a09997e36441f863f7 |
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| Source note | uspto-grants-2011_05 |
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