HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596467Generated: October 31, 2026
Thionyl Chloride → HCID 12674604, compound
https://huagongshe.com/reaction/596467
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 12674602 | HCID 12674602 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 12674604 | HCID 12674604 | 94% |
Reaction Steps
To a solution of 16 g. of 1-(p-chlorophenyl)-3-(1-(hydroxymethyl)ethyl)-4-methyl-2-imidazolidinone in 400 ml. of anhydrous chloroform, 14.5 g. of SOCl2 is added dropwise with stirring while the temperature is maintained at 0° C. The mixture is then refluxed for 45 minutes, concentrated under vacuum and taken up with benzene, then evaporated to dryness again, yielding 15.1 grams (94%) of the title compound, m.p. 70°-72° C. (from diisopropyl ether). The corresponding m-chlorophenyl-substituted compound is prepared in the same way. Yield 97%, b.p. 200° C./0.5 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04011238 |
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| Source dataset | uspto-grants-1977_03 |
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| ORD ID | ord-f5644c9186be45f1b9adf60775f67dff |
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| Source note | uspto-grants-1977_03 |
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