HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127483Generated: November 2, 2026
Benzene → 2,2-Dichloro-1-(1-thia-4-azaspiro[4.5]decan-4-yl)ethan-1-one
https://huagongshe.com/reaction/127483
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Cysteamine | HCID 6058 | — |
| Reactant | Dichloroacetyl chloride | HCID 6593 | — |
| Reactant | Cyclohexanone | HCID 7967 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,2-Dichloro-1-(1-thia-4-azaspiro[4.5]decan-4-yl)ethan-1-one | HCID 13277203 | — |
Reaction Steps
From a boiling mixture of 9.8 g. (0.1 moles) of cyclohexanone and 7.7 g. (0.1 moles) of 2-mercaptoethylamine in 100 ml. of benzene the water formed is continuously distilled off. Boiling is continued until 1.8 ml. of water are separated. The reaction mixture is then cooled and 11 g. of a 40% aqueous sodium hydroxide solution are added followed by dropwise addition of 14.7 g. (0.1 moles) of dichloroacetyl chloride, with external salt/ice cooling. Mixture is stirred for a further two hours at room temperature and washed with aqueous hydrochloric acid solution and subsequently with water. From the neutral mixture obtained benzene is distilled off in vacuo to give 17.2 g. (0.064 moles) of a white powder. Recrystallization from absolute ethanol yields a white crystalline product melting at 149° to 151° C. The structure of the named compound can be verified by IR spectrum analysis.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04256481 |
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| Source dataset | uspto-grants-1981_03 |
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| ORD ID | ord-c9ccf6a9241a4f148b83292be52195c3 |
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| Source note | uspto-grants-1981_03 |
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