HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231684Generated: October 31, 2026
Hydrochloric Acid → HCID 20033663, compound
https://huagongshe.com/reaction/231684
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | HCID 20033724 | HCID 20033724 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20033663 | HCID 20033663 | 44% |
Reaction Steps
To 5-(4-hydroxyphenylsulfonyl)-4-methylthiophene-2-sulfonamide (2.0 g, 0.006 mol) in ethanol (10 ml) was added 40% aqueous dimethylamine (2.7 g, 0.024 mol) followed by 37% aqueous formaldehyde (0.59, 0.0072 mol). The solution was stirred in an oil bath (98° C.) for 161/2 hours. The solvent was removed in vacuo. The residual oil was taken up in ethyl acetate and extracted with dilute HCl. The HCl extract was basified with NaHCO3 and the product was extracted into ethyl acetate. The extract was washed with water, dried, filtered and concentrated in vacuo. This procedure gave a solid foam in 44% yield which was converted to the hydrochloride salt with ethanolic HCl. The white solid HCl salt melted at 262°-263° C. Purity and structure were confirmed by C, H, N analyses, HPLC and NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04847289 |
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| Source dataset | uspto-grants-1989_07 |
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| ORD ID | ord-803bb1072de64e6292337357419c628c |
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| Source note | uspto-grants-1989_07 |
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