HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2045772Generated: October 30, 2026
Diisopropylethylamine → HCID 57424364, compound
https://huagongshe.com/reaction/2045772
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 10353361 | HCID 10353361 | — |
| Reactant | 3-Iodo-2-(iodomethyl)prop-1-ene | HCID 11045029 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57424364 | HCID 57424364 | — |
Reaction Steps
A mixture of 3-chloro-2-(chloromethyl)prop-1-ene (1.0 g, 8 mmol) and sodium iodide (6.6 g, 44 mmol) in acetone (60 mL) was stirred at room temperature for 20 hours, evaporated under reduced pressure and dissolved in dichloromethane (150 mL) and water (50 mL). The organic layer was dried over sodium sulfate, filtered and evaporated to yield 3-iodo-2-(iodomethyl)prop-1-ene as a reddish oil (2.45 g). N,N-diisopropylethylamine (0.20 mL) was added to a solution of 2-nitro-1-(2,4,5-trifluorophenyl)ethanone (110 mg, 0.5 mmol) in N,N-dimethylformamide (3 mL) and 3-iodo-2-(iodomethyl)prop-1-ene (170 mg, 0.55 mmol) and the mixture was heated at 60° C. for 2.5 hours, evaporated and purified by chromatography on a Biotage Horizon® system (silica, gradient 0-30% dichloromethane in hexane) to yield 3-methylene-5-nitro-6-(2,4,5-trifluorophenyl)-3,4-dihydro-2H-pyran.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08592371B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-1554331228174feeb4002880e4d53f08 |
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| Source note | uspto-grants-2013_11 |
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