HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393027Generated: October 30, 2026
Sulfamic Acid → 3-Chloro-4-hydroxy-5-methylbenzoic acid
https://huagongshe.com/reaction/393027
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfamic Acid | HCID 5987 | — |
| Reactant | 3-Chloro-4-hydroxy-5-methylbenzaldehyde | HCID 22661382 | — |
| Reactant | Sodium Chlorite | HCID 23668197 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 3-Chloro-4-hydroxy-5-methylbenzoic acid | HCID 22661331 | 52% |
Reaction Steps
A solution of sulfamic acid (11.8 g, 121.5 mmol) in water (25 mL) was added with vigorous stirring to 3-chloro-4-hydroxy-5-methylbenzaldehyde (16.00 g, 93.8 mmol) in tert-butanol (100 mL). The mixture was cooled (˜12° C.) and a solution of sodium chlorite (12.00 g, 106.1 mmol) in water (25 mL) was added in 5 mL portions with vigorous stirring. The reaction was exothermic and the temperature at the end of the addition was approximately 50° C. The two layers were separated and the aqueous layer was extracted with ether (2×50 mL). The organic layers were washed with brine and evaporated to dryness. Water was added, and the mixture was stirred and filtered. The solid was dissolved in warm ether (250 mL), and the solution was dried, filtered, concentrated to 100 mL, and cooled in the freezer (approx. −20° C.). Filtration and washing with cold ether gave 3-chloro-4-hydroxy-5-methylbenzoic acid (9.10 g, 52%), as a yellow solid, mp 242-244° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06803384B2 |
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| Source dataset | uspto-grants-2004_10 |
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| ORD ID | ord-52d501dbc7e548cc8b34ed37582ebe21 |
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| Source note | uspto-grants-2004_10 |
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