HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 262411Generated: November 3, 2026
Hydrochloric Acid → HCID 21318665, compound
https://huagongshe.com/reaction/262411
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 21318677 | HCID 21318677 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21318665 | HCID 21318665 | — |
Reaction Steps
A 0.55 g. sample of N-(4,5,6,7-tetrahydro-4-oxobenzo[b]thien-7-yl)phthalimide is stirred and heated at reflux with 5 ml. of 6N HCl and one ml. of ethanol for 16 hours. Subsequently, the ethanol is distilled off and refluxing is continued for another 4 hours with the addition of 2 ml. of concentrated HCl. The mixture is cooled in ice, the white crystals of phthalic acid are filtered and washed with 5 ml. of water. The filtrate is washed with 15 ml. of CHCl3 and the aqueous solution of 4,5,6,7-tetrahydro-4-oxobenzo[b]thiophen-7-amine hydrochloride is neutralized until the solution is at pH 10-11 with 50% aqueous NaOH. The amine is then extracted from the aqueous mixture with chloroform (3×25 ml.). The combined extracts are dried over MgSO4 and evaporated to afford 0.17 g. of light yellow syrup. This gives the title compound with infrared absorption bands at 1660, 1620 and 1520 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04154740 |
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| Source dataset | uspto-grants-1979_05 |
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| ORD ID | ord-1650b478c4e2431384b5346ddf58a7df |
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| Source note | uspto-grants-1979_05 |
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