HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096401Generated: October 30, 2026
Lawesson's reagent → HCID 58423803, compound
https://huagongshe.com/reaction/2096401
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lawesson's reagent | HCID 87949 | — |
| Reactant | HCID 58424173 | HCID 58424173 | — |
| Solvent | M-Xylene | HCID 7929 | — |
| Product | HCID 58423803 | HCID 58423803 | 74% |
Reaction Steps
A suspension of 6-bromo-2-(2,3-difluorophenyl)spiro[chroman-4,4′-imidazolidine]-2′,5′-dione (212 mg, 0.52 mmol) and Lawesson's Reagent (201 mg, 0.52 mmol) in dry m-xylene (4.5 mL) was heated at 150° C. in a 10 mL CEM microwave test tube for 25 minutes. The mixture was concentrated in vacuo and the residue was purified by preparative TLC to give 6-bromo-2-(2,3-difluorophenyl)-2′-thioxospiro[chroman-4,4′-imidazolidine]-5′-one (163 mg, 74%). 1H-NMR (CDCl3): 2.33 (t, 3H), 2.54 (d, 1H), 5.36 (s, 1H), 6.17 (d, 1H), 6.91 (d, 1H), 7.17 (m, 3H), 7.30 (m, 2H), 7.46 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08450308B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-22b44d9039c4458eb994e895fec98dcf |
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| Source note | uspto-grants-2013_05 |
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