HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257355Generated: October 25, 2026
Formaldehyde → 4-Chloro-2-hydroxybenzaldehyde
https://huagongshe.com/reaction/257355
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | 3-Chlorophenol | HCID 7933 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Hexamethylphosphoramide | HCID 12679 | — |
| Reactant | HCID 178418443 | HCID 178418443 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-Chloro-2-hydroxybenzaldehyde | HCID 520101 | 73.5% |
Reaction Steps
A 2M solution of ethylmagnesium bromide in tetrahydrofuran (50 ml, 0.10 mole) was placed in a flask, and a solution of 12.85 g (0.10 mole) of 3-chlorophenol in 50 mL of diethyl ether was added slowly with stirring. The addition required two hours, after which the solvents were removed by evaporation under reduced pressure. Toluene (200 ml), 7.50 g (0.25 mole) of paraformaldehyde, and 17.92 g (0.10 mole) of hexamethylphosphoramide were added to the residue, and this mixture was heated at 80° C. for approximately 16 hours. The solvent was evaporated under reduced pressure, leaving a residue. This residue was washed successively with 50 mL of hydrochloric acid and 300 mL of water. Vacuum distillation of the washed residue yielded 11.50 g of 4-chlorosalicylaldehyde, b.p. 112° C. at 9 mm of Hg. This reaction was repeated several times.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05262390 |
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| Source dataset | uspto-grants-1993_11 |
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| ORD ID | ord-e8df0bebc4294be48db9951d1906c2d9 |
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| Source note | uspto-grants-1993_11 |
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