HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370121Generated: October 28, 2026
4-Hydroxybenzaldehyde → 3-Chloro-4-hydroxybenzaldehyde
https://huagongshe.com/reaction/1370121
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-Chloro-4-hydroxybenzaldehyde | HCID 17022 | 66.9% |
Reaction Steps
To a solution of 4-hydroxybenzaldehyde (100 g) in chloroform (1 L) was added N-chlorosuccinimide (120 g) at ambient temperature and the mixture was stirred at 50° C. for 18 hours. After evaporation of the solvent, the residue was partitioned between ethyl acetate and water. The organic layer was washed with water and brine, dried over magnesium sulfate, and evaporated in vacuo. The crude crystals was washed with diisopropyl ether and recrystallized from a mixture of ethyl acetate and n-hexane to obtain 3-chloro-4-hydroxybenzaldehyde (85.8 g) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06582351B1 |
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| Source dataset | uspto-grants-2003_06 |
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| ORD ID | ord-1686a51d80934a25b5050ed27cf628cc |
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| Source note | uspto-grants-2003_06 |
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