HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 932153Generated: November 1, 2026
Diisopropyl bromomethylphosphonate → HCID 11322769, compound
https://huagongshe.com/reaction/932153
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropyl bromomethylphosphonate | HCID 4366885 | — |
| Reactant | Potassium ethanethioate | HCID 23670855 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 11322769 | HCID 11322769 | — |
Reaction Steps
To a stirred solution of diisopropyl bromomethylphosphonate (5.00 g, 19.3 mmol) in N,N-dimethylformamide (15.4 mL) was added potassium thioacetate (3.75 g, 32.8 mmol) followed by tetrabutylammonium iodide (0.36 g, 0.97 mmol). The reaction mixture was stirred at 85° C. for 2.5 hours. The reaction mixture was cooled and partitioned between water and EtOAc (3×) and the layers were separated. The combined organic layers were dried over Na2SO4, filtered and the filtrate was concentrated under reduced pressure. Purification of the residue by flash chromatography on silica gel (24 g column, eluent: 0 to 90% EtOAc/hexanes) provided the title compound as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09296736B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-f4895425ac504855a9924cd6e64eedb8 |
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| Source note | uspto-grants-2016_03 |
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