HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899571Generated: October 29, 2026
3-Phenoxybenzaldehyde → HCID 16735089, compound
https://huagongshe.com/reaction/899571
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Phenoxybenzaldehyde | HCID 38284 | — |
| Reactant | HCID 178506676 | HCID 178506676 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 16735089 | HCID 16735089 | 86% |
Reaction Steps
To a stirred solution of 3-phenoxybenzaldehyde (2 g, 10.09 mmol) in THF (15 mL) at −78° C. was added phenyllithium (6.73 mL, 1.8M solution in cyclohexane-ether) dropwise. After stirring under argon at −78° C. for 4 hrs, the reaction was quenched with water and extracted with diethyl ether. The organic layer was washed with brine, dried with magnesium sulfate, filtered, and concentrated under reduced pressure to give the crude product. The crude mixture was purified via flash SiO2 chromatography (ethyl acetate/hexanes (10%/90%) to (20%/80%)) to give 128 (2.79 g, 86% yield): 1H-NMR (400 MHz, chloroform-d) δ 6.87-7.38 (m, 10H), 7.09 (m, 1H), 6.99 (app d, J=7.3 Hz, 1H), 6.88 (m, J=8.6, 2.2 Hz, 1H), 5.81 (s, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07355079B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-53217933de584f818423054191ac2417 |
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| Source note | uspto-grants-2008_04 |
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