HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259336Generated: October 29, 2026
Hydrochloric Acid → 4,5,6,7-Tetrahydro-7-oxobenzo[b]thiophen-4-amine hydrochloride
https://huagongshe.com/reaction/259336
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | N-(7-Oxo-4,5,6,7-tetrahydro-1-benzothiophen-4-yl)formamide | HCID 23347790 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4,5,6,7-Tetrahydro-7-oxobenzo[b]thiophen-4-amine hydrochloride | HCID 23347795 | — |
Reaction Steps
A mixture of (+)-N-(4,5,6,7-tetrahydro-7-oxobenzo[b]thien-4-yl)formamide (52.65 grams) in 525 ml. of 95% ethanol and 525 ml. of 2N HCl is heated at reflux for 2 hours. The mixture is cooled, filtered through glass wool and the filtrate is evaporated to dryness. The dark solid is dissolved in 180 ml. of water and the insoluble material is collected by filtration. The filter cake is washed with 70 ml. of water and the combined solution containing the title compound is used in the next operation. A 3 ml. solution is evaporated to dryness and the residue is dissolved in 95% ethanol. The ethanol solution is decolorized with activated carbon and filtered. The filtrate is evaporated to dryness to afford 0.5 grams of the title compound, m.p. 212°-214° C. (dec.), [α]D26 = + 13.56° (c, 0.59 in methanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04036979 |
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| Source dataset | uspto-grants-1977_07 |
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| ORD ID | ord-65f9a4dd961149b893cec5e0b18b340c |
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| Source note | uspto-grants-1977_07 |
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