HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172807Generated: November 2, 2026
m-Chloroperbenzoic acid → 4-(4-Chlorophenoxy)phenol
https://huagongshe.com/reaction/1172807
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-(4-chlorophenoxy)benzaldehyde | HCID 2767675 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(4-Chlorophenoxy)phenol | HCID 12346120 | — |
Reaction Steps
The crude aldehyde from step 1 (23.3 g, 0.10 mmol) was dissolved in dichloromethane (500 mL), and m-chloroperbenzoic acid (70%, 50.0 g, 0.20 mmol) and sodium bicarbonate (25.2 g, 0.30 mmol) were added. The resulting heterogeneous mixture was stirred and heated under reflux for 2 h and then quenched with an aqueous solution of sodium sulfite (0.5 M, 500 mL). After stirring at 25° C. for 30 min, the organic phase was separated and the aqueouse phase was extracted with dichloromethane (2×200 mL). The combined organic phases were washed with a saturated solution of sodium bicarbonate (2×200 mL), dried over magnesium sulfate and concentrated. The residue was chromatographed on silica gel, eluting with an 8:2 mixture of hexane and ethyl acetate to give the title phenol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07834036B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-a7609a2c0e894ae69e3c8b6a2de92cba |
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| Source note | uspto-grants-2010_11 |
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