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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1254011Generated: November 4, 2026

Diisopropylethylamine → HCID 57424364, compound

https://huagongshe.com/reaction/1254011

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 10353361HCID 10353361—
Reactant3-Iodo-2-(iodomethyl)prop-1-eneHCID 11045029—
SolventDimethylformamideHCID 6228—
ProductHCID 57424364HCID 57424364—

Reaction Conditions

Temperature60 °C

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 h, 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. 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 h, evaporated and purified by chromatography on a Biotage Horizon® system (silica gel, gradient 0-30% dichloromethane in hexane) to yield 3-methylene-5-nitro-6-(2,4,5-trifluorophenyl)-3,4-dihydro-2H-pyran.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455533B2
Source datasetuspto-grants-2013_06
ORD IDord-9c0cc2dd638d48859087fb664ac2fcd0
Source noteuspto-grants-2013_06