HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922256Generated: November 1, 2026
Tributylphosphine → 2-[4-[[4-[(2Z)-2-methoxyimino-2-phenylethoxy]phenyl]methoxy]phenyl]acetonitrile
https://huagongshe.com/reaction/922256
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tributylphosphine | HCID 13831 | — |
| Reactant | 4-Hydroxybenzyl cyanide | HCID 26548 | — |
| Reactant | 2-(4-Hydroxymethyl-phenoxy)-1-phenyl-ethanone O-methyl-oxime | HCID 86695760 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-[4-[[4-[(2Z)-2-methoxyimino-2-phenylethoxy]phenyl]methoxy]phenyl]acetonitrile | HCID 88581336 | 62.9% |
Reaction Steps
To a 50 mL RB flask fitted with magnetic stirrer was charged dry Toluene. To the stirred solvent was added 2-(4-Hydroxymethyl-phenoxy)-1-phenyl-ethanone O-methyl-oxime (0.20 g, 0.74 mmol) and (4-hydroxyphenyl)acetonitrile (0.098 g, 0.74 mmol) at 0° C. for 5 min. Then added tributylphosphine (0.0.24 g, 1.2 mmol) stirred at 0° C. for 15 min, was added 1,1′aza(dicarbonyl)dipiperidine (0.303 g, 1.2 mmol), this resulting mass stirred at RT for 16 h, The solvent removed, the residue was extracted with ethyl acetate. The organic layer washed with water and brine solution and dried by anhydrous sodium sulphate and evaporated, purified by 100-200 silica column using pet-ether and ethylacetate. The product obtained as a colourless oily liquid (0.18 g, 60.00%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09278915B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-561d14d2a1594c90b5077b7fb9c65d25 |
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| Source note | uspto-grants-2016_03 |
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