HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 263211Generated: October 27, 2026
Urea → N-(4,5,6,7-Tetrahydro-1-benzothiophen-4-yl)urea
https://huagongshe.com/reaction/263211
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Urea | HCID 1176 | — |
| Reactant | 4-Hydroxy-4,5,6,7-tetrahydrobenzo[b]thiophene | HCID 13911631 | — |
| Reactant | 4-Chloro-4,5,6,7-tetrahydrobenzo[b]thiophene | HCID 20348922 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Solvent | Diisopropylethylamine | HCID 81531 | — |
| Product | N-(4,5,6,7-Tetrahydro-1-benzothiophen-4-yl)urea | HCID 13036998 | — |
Reaction Steps
A 1 gram sample of 4-hydroxy-4,5,6,7-tetrahydrobenzo[b]thiophene is stirred in the cold for several hours in thionyl chloride (5 ml.) and the mixture is evaporated to dryness. The crude 4-chloro-4,5,6,7-tetrahydrobenzo[b]thiophene is then added to a mixture of urea (1-5 mole-equivalents) in dimethylformamide and diisopropyl ethylamine. The mixture is warmed, after several hours, to 50° C. and after 4 hours is poured on ice and the product, 4,5,6,7-tetrahydrobenzo[b]thien-4-ylurea, is collected by filtration.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04156670 |
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| Source dataset | uspto-grants-1979_05 |
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| ORD ID | ord-fa99fafdac9143eaad5a0de2ff22cd4a |
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| Source note | uspto-grants-1979_05 |
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