HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 749539Generated: October 29, 2026
Hydrochloric Acid → HCID 22235003, compound
https://huagongshe.com/reaction/749539
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Iodobenzyl bromide | HCID 954258 | — |
| Reactant | 2-(3,3,3-Trifluoropropyl)malononitrile | HCID 22185761 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22235003 | HCID 22235003 | 22.9% |
Reaction Steps
First, 0.55 g of 4-iodobenzyl bromide was dissolved in 10 ml of N,N-dimethylformamide, to which the suspension of 0.11 g of sodium hydride (60% in oil) and 0.30 g of (3,3,3-trifluoropropyl)malononitrile in 5 ml of N,N-dimethylformamide was added dropwise, while stirring under ice cooling. After stirring for 4 hours at 0° C., 10% hydrochloric acid was added to the reaction mixture at room temperature, which was extracted with ethyl acetate. The organic layer was successively washed with water, a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 0.16 g of 2-(4-iodobenzyl)-2-(3,3,3-trifluoropropyl)malononitrile (the present compound (26)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07402691B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-cec7e3d79eb444efa059ed3cab5c61a5 |
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| Source note | uspto-grants-2008_07 |
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