HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971969Generated: October 29, 2026
3-Phenoxybenzaldehyde → HCID 88794023, compound
https://huagongshe.com/reaction/971969
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Phenoxybenzaldehyde | HCID 38284 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Catalyst | Triethylamine hydrochloride | HCID 11130 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 88794023 | HCID 88794023 | 98.5% |
Reaction Steps
To a solution prepared by dissolving 1.3 g of triethylamine hydrochloride (0.009 mole) in 69.2 g of a 35.8% aqueous solution of sodium bisulfite (0.238 mole of sodium bisulfite) while being stirred at room temperature, was added dropwise taking 2 hours a solution prepared by dissolving 50 g of crude 3-phenoxybenzaldehyde (72.5% purity (0.183 mole of 3-phenoxybenzaldehyde) and containing no other aldehyde compounds) in 80 g of toluene. Immediately after the starting of the dropwise addition, white crystals began to precipitate out of the reaction system. After completion of the addition, stirring was continued for a further 2 hours. The crystals were collected by filtration, washed three times with 50 g of toluene, and dried to obtain 54.5 g (98.5% yield) of 3-phenoxybenzaldehyde sodium bisulfite adduct.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04162269 |
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| Source dataset | uspto-grants-1979_07 |
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| ORD ID | ord-21142b84db1041cba4690710a20342ec |
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| Source note | uspto-grants-1979_07 |
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