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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244258Generated: October 30, 2026

1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene) → HCID 15546053, compound

https://huagongshe.com/reaction/244258

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene)HCID 96831—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 15546052HCID 15546052—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
ProductHCID 15546053HCID 1554605366%

Reaction Steps

To Compound 7 (140 mg, 0.53 mmol), anhydrous pyridine was added, followed by performing azeotropy of the mixture 3 times. Then, the product was converted into an anhydrous pyridine solution (1.5 ml), and 4,4′-dimethoxytrityl chloride (210 mg, 0.63 mmol) and DMAP (6.5 mg, 0.053 mmol) were added at room temperature in a stream of nitrogen. The mixture was stirred for 5 hours at room temperature. To the reaction mixture, a saturated sodium bicarbonate solution was added, followed by extraction with CH2Cl2. The organic phase was washed with water and a saturated sodium chloride solution, and then dried over anhydrous sodium sulfate. After the solvents were distilled off under reduced pressure, the resulting crude product was purified by silica gel column chromatography (CHCl3:MeOH=40:1) to obtain Compound 8 (230 mg, 0.34 mmol, 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE044779E1
Source datasetuspto-grants-2014_02
ORD IDord-6411048d47b440de883baf86cecdaa86
Source noteuspto-grants-2014_02