HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626313Generated: October 29, 2026
Triphenylphosphine → HCID 117620473, compound
https://huagongshe.com/reaction/626313
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | (1-Methylcyclopropyl)methanol | HCID 137701 | — |
| Reactant | 2,5-Dimethyl-4-nitrophenol | HCID 282110 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-methoxyethyl N-(2-methoxyethoxycarbonylimino)carbamate | HCID 53384415 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 117620473 | HCID 117620473 | 34.8% |
Reaction Steps
2.98 g of Bis(2-methoxyethyl) azodicarboxylate was added to a mixture of 1.59 g of 2,5-dimethyl-4-nitrophenol, 0.81 g of (1-methylcyclopropyl)methanol, 2.98 g of triphenylphosphine and 50 mL of toluene at 0° C., and the mixture was stirred at 80° C. for 4 hours. After cooling, a saturated aqueous sodium bicarbonate solution was added, and the mixture was extracted with ethyl acetate, and then the organic layer was washed with water and saturated salt water and dried over anhydrous magnesium sulfate. The resulting residue was subjected to silica gel column chromatography to obtain 0.77 g of 2,5-dimethyl-1-[(1-methylcyclopropyl)methoxy]-4-nitrobenzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09309191B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-8197e26fd9fb4a45b3da0a84633bde23 |
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| Source note | uspto-grants-2016_04 |
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