HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131093Generated: October 25, 2026
Sodium hydride → 2',3'-Dinitro-3,4,4',5-tetramethoxy-(Z)-stilbene
https://huagongshe.com/reaction/131093
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Triphenyl(3,4,5-trimethoxybenzyl)phosphonium bromide | HCID 370917 | — |
| Reactant | 4-Methoxy-2,3-dinitrobenzaldehyde | HCID 22349243 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2',3'-Dinitro-3,4,4',5-tetramethoxy-(Z)-stilbene | HCID 24854190 | 51% |
Reaction Steps
4-methoxy-2,3-dinitrobenzaldehyde (2.94 mmol) and 3,4,5-trimethoxybenzyltriphenyl phosphonium bromide (1.54 g, 2.94 mmol, 1.0 equiv) in anhydrous dichloromethane (25 mL) was added NaH (0.424 g, 17.67 mmol, 6.0 equiv). The reaction mixture was stirred at room temperature for about 7 hours and monitored by TLC. The reaction was quenched by adding water, the organic layer was separated and the aqueous layer was extracted with dichloromethane (3×25 mL). The combined organic layer was washed with brine, dried over Na2SO4 and concentrated in vacuo to orange colored slush. To this was added about 15 mL of dichloromethane and refrigerated overnight. The crude mixture was subjected to flash chromatography to isolate 2′,3′-Dinitro-3,4,4′,5-tetramethoxy-(Z)-stilbene (0.581 g, 1.48 mmol, 51%, solid)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07384925B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-450daebe13584f93b88af5344be92bb9 |
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| Source note | uspto-grants-2008_06 |
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