HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678752Generated: October 29, 2026
Tetrahydrofuran → 1-(4-(1,3-Dioxolan-2-yl)phenyl)-2-phenylethanone
https://huagongshe.com/reaction/1678752
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4-(1,3-Dioxolan-2-yl)benzonitrile | HCID 2778428 | — |
| Reactant | HCID 178418336 | HCID 178418336 | — |
| Product | 1-(4-(1,3-Dioxolan-2-yl)phenyl)-2-phenylethanone | HCID 59164356 | — |
Reaction Steps
To a solution of 4-(1,3-dioxolan-2-yl)benzonitrile (5.0 g, 28.54 mmol) in anhydrous THF (100 mL) was added benzyl magnesium chloride (36 mL, 20% wt solution in THF, 43 mmol) slowly at 0° C. After one hour the mixture was warmed to room temperature. After four hours the mixture was cooled to 0° C. and quenched with saturated NH4Cl. The mixture was warmed to room temperature and extracted with ethyl acetate (3×). The combined organic layers were dried (MgSO4), filtered, and concentrated. Flash column chromatography (10% ethyl acetate/hexanes) gave 1-[4-(1,3-dioxolan-2-yl)phenyl]-2-phenylethanone as a pale yellow solid: 1H-NMR (500 MHz, CDCl3): δ 8.02 (2H, d, J=8.30 Hz,), 7.57 (2H, d, J=8.30 Hz,), 7.38-7.24 (5H, m), 5.86 (1H, s), 4.29 (2H, s), 4.28-4.09 (4H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08008317B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-5bfe6e5708b148ffa130485472a5ed45 |
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| Source note | uspto-grants-2011_08 |
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