HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 861272Generated: October 30, 2026
Tetrahydrofuran → HCID 54192599, compound
https://huagongshe.com/reaction/861272
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | [(4-Nitrophenyl)methyl](triphenyl)phosphanium bromide | HCID 197008 | — |
| Reactant | HCID 19702707 | HCID 19702707 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 54192599 | HCID 54192599 | — |
Reaction Steps
A mixture of 3-allyl-4-(N-allyl-N-methylamino)benzaldehyde (10.25 g, 0.05 mol), THF (100 ml), p-nitrobenzyl triphenylphosphonium bromide (27.4 g, 0.55 mol) and water (50 ml) is mixed at room temperature while 2M sodium carbonate solution (50 ml) is added over 5 minutes. The mixture is stirred mechanically for 2 hours. The mixture is diluted with water (300 ml) and extracted two times with ether (50 ml portions). The extracts are washed with water and brine, dried over magnesium sulfate and concentrated. The mixture is diluted with toluene (100 ml) and hexane (200 ml) and the triphenyl phosphine oxide filtered off. The filtrate is concentrated and chromatographed on silica with hexane-ethyl acetate to give pure N,2-diallyl-N-methyl-4-[2-(4-nitrophenyl)ethenyl]aniline.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05714304 |
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| Source dataset | uspto-grants-1998_02 |
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| ORD ID | ord-695758386f9946d486a5f544a3202460 |
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| Source note | uspto-grants-1998_02 |
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