HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 993138Generated: October 29, 2026
Hydrochloric Acid → HCID 22890467, compound
https://huagongshe.com/reaction/993138
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Nitrobenzene | HCID 7416 | — |
| Reactant | 3,4-Diethoxyphenol | HCID 14450310 | — |
| Reactant | HCID 22890470 | HCID 22890470 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Product | HCID 22890467 | HCID 22890467 | — |
Reaction Steps
Nitrobenzene (100 ml) was cooled to zero degrees Celsius and saturated with HCl gas. To this solution was added of 3,4-diethoxy-phenol (11.64 g, 64 mmoles), propane-1-sulfonic acid cyanomethyl-amide (10.36 g, 64 mmoles) and zinc chloride (17.45 g, 128 mmoles). The reaction was stirred for 1 hour at zero degrees Celsius and then allowed to warm to room temperature. Stirring was continued for 2 hours. Thin-layer chromatography showed consumption of 3,4-diethoxy-phenol. Water (100 ml) was added cautiously and the reaction was heated to 100 degrees Celsius for 1 hour. The reaction was cooled, and extracted with methylene chloride. The extracts were washed with water, brine, dried over anhydrous sodium sulfate, filtered, and the solvent was removed in vacuo. The residue was submitted to flash chromatography (2.5-5% ethyl acetate in methylene chloride). The purified product was triturated with ether, filtered and air dried to yield 17.3 g of propane-1-sulfonic acid [2-(4,5-diethoxy-2-hydroxy-phenyl)-2-oxo-ethyl]-amide. 1HNMR (CDCl3): 11.86 (s, 1H), 6.93 (s, 1H), 6.46 (s, 1H), 5.26 (t, 1H), 4.55 (d, 2H), 4.14 (q, 2H), 4.03 (q, 2H), 3.05 (m, 2H), 1.90 (m, 2H), 1.45 (m, 6H), 1.07 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06472393B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-cddc3b136ed842fbab59f26dae159741 |
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| Source note | uspto-grants-2002_10 |
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