HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857482Generated: October 29, 2026
Methoxymethyl-triphenylphosphonium chloride → HCID 69411264, compound
https://huagongshe.com/reaction/857482
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methoxymethyl-triphenylphosphonium chloride | HCID 2723798 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | HCID 86594822 | HCID 86594822 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69411264 | HCID 69411264 | — |
Reaction Steps
To a solution of (methoxymethyl)triphenylphosphonium chloride (533 mg, 1.55 mmol) in THF (10 ml) at 0° C. was added lithium hexamethyldisilazide (1.55 ml, 1M solution, 1.55 mmol). The reaction mixture was stirred for 0.5 h and cooled to −78° C. A solution of 2-(4-chloro-phenyl)-1-(2-chloro-phenyl)-5-formyl-1H-imidazole-4-carboxylic acid ethyl ester I-5e (408 mg, 1.05 mmol) in THF (5 ml) was slowly added via cannula. The reaction mixture was stirred at −78° C. for 5 min, then was allowed to warm to room temperature and stir for 3 hours. The reaction mixture was quenched with H2O and diluted with EtOAc. The organic solution was separated and the aqueous layer was extracted once with EtOAc. The combined EtOAc extracts were washed with sat'd aq. NaCl, dried, and concentrated in vacuo. The crude residue was purified on 4 mm chromatotron plates using 1:1 EtOAc/hexanes to give the product (I-5g) as two isomeric compounds (148 mg, 34% and 157 mg, 36%): +APCI MS (M+1) 417.2
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07145012B2 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-37aff48aaad34137b08505d5a9301905 |
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| Source note | uspto-grants-2006_12 |
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