HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1959116Generated: November 3, 2026
Acetic acid, 2-(triphenylphosphoranylidene)-, methyl ester → HCID 59442983, compound
https://huagongshe.com/reaction/1959116
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic acid, 2-(triphenylphosphoranylidene)-, methyl ester | HCID 17453 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 10060688 | HCID 10060688 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 59442983 | HCID 59442983 | — |
Reaction Steps
Under argon atmosphere, a mixture of (4-chloro-2-hydroxyphenyl)(4-fluorophenyl)methanone (1.00 and methyl(triphenylphosphoranylidene)acetate (3.00 g) in toluene (15 mL) was heated under reflux for 15 hours. After cooling, the reaction solution was poured into a saturated aqueous solution of ammonium chloride and the mixture was extracted with ethyl acetate. The organic layer was washed successively with a saturated aqueous solution of sodium bicarbonate and brine, dried over sodium sulfate and concentrated in vacuo. The resultant residue was purified by column chromatography on silica gel (Solvent: n-hexane/ethyl acetate=95/5 to 85/15) and the product was triturated in n-hexane-diisopropyl ether to give the titled compound (0.54 g) as a pale yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08410166B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-8bbc661bdd1c4964adf5932aa49e4ceb |
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| Source note | uspto-grants-2013_04 |
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