HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250735Generated: November 2, 2026
Hydrochloric Acid → p-Toluenesulfinic acid
https://huagongshe.com/reaction/250735
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium p-toluenesulfinate | HCID 2723791 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | p-Toluenesulfinic acid | HCID 10818 | 98.8% |
Reaction Steps
Treat a solution of p-toluenesulfinic acid sodium salt, (6.0 g, 33.7 mmol) in water (20 mL) and tert-butyl methyl ether (10 mL) dropwise with concentrated HCl (3 mL) and stir for 10 minutes. Separate the solution in a separatory funnel and wash the organic layer with saturated aqueous sodium chloride. Dry the organic over Na2SO4, filter, and remove the solvent to afford 5.2 g (quantitative) of p-toluenesulfinic acid. Combine the acid with benzaldehyde (2.4 g, 22.5 mmol), formamide (3.8 g, 84.2 mmol), and trimethylsilyl chloride (4.0 g, 37.0 mmol) in 30 mL of a 1:1 solution of toluene/acetonitrile. Heat the reaction to 50° C. and stir for 5 hours. Cool the reaction and dilute with water (100 mL) and tert-butyl methyl ether (30 mL). Cool the solution in an ice bath and filter to afford 4.5 g (70%) of desired product. Dry the solid under vacuum overnight to remove any residual water.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07863310B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-b2d56c59c4ef4b45a4d5562a524e069b |
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| Source note | uspto-grants-2011_01 |
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