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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1294847Generated: October 30, 2026

Methoxymethyl-triphenylphosphonium chloride → HCID 69411264, compound

https://huagongshe.com/reaction/1294847

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethoxymethyl-triphenylphosphonium chlorideHCID 2723798—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 86594822HCID 86594822—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69411264HCID 69411264—

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241788B2
Source datasetuspto-grants-2007_07
ORD IDord-68558a232c674c4a9f6e6d42bd2998de
Source noteuspto-grants-2007_07