HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626318Generated: October 26, 2026
Triphenylphosphine → HCID 117620575, compound
https://huagongshe.com/reaction/626318
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2,5-Dimethyl-4-nitrophenol | HCID 282110 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2,2,3,3-Tetramethylcyclopropanemethanol | HCID 544179 | — |
| Reactant | 2-methoxyethyl N-(2-methoxyethoxycarbonylimino)carbamate | HCID 53384415 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 117620575 | HCID 117620575 | 8.4% |
Reaction Steps
1.97 g of Bis(2-methoxyethyl) azodicarboxylate was added to a mixture of 1.08 g of 2,5-dimethyl-4-nitrophenol, 0.83 g of (2,2,3,3-tetramethylcyclopropyl)methanol, 2.04 g of triphenylphosphine and 100 mL of toluene at 0° C., and the mixture was stirred at 90° 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 0.15 g of 2,5-dimethyl-4-nitro-1-[(2,2,3,3-tetramethylcyclopropyl) methoxy]benzene.
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-23c8524c408f49c9a356b4fac06ecd9e |
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| Source note | uspto-grants-2016_04 |
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