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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736858Generated: November 2, 2026

Dichloromethane → HCID 86626449, compound

https://huagongshe.com/reaction/736858

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 86626450HCID 86626450—
SolventPyridineHCID 1049—
SolventChloroformHCID 6212—
SolventEthyl AcetateHCID 8857—
ProductHCID 86626449HCID 8662644972.4%

Reaction Steps

1,1′-[(1E,3E)-2,3-diformylamino-1,3-butadiene-1,4-diyl]bis[methoxybenzene] (3.4 mg, 0.0096 mmol) prepared in Reference Synthetic Example 6 was suspended in chloroform (100 μl) and pyridine (100 μl), and a dichloromethane solution of phosphorus oxychloride (2 μl, 0.021 mmol) was dropwise added under cooling with ice. After stirring for 30 minutes, the suspension was diluted with ethyl acetate and poured into a saturated sodium hydrogen carbonate aqueous solution. Extraction with ethyl acetate was carried out twice, and the obtained organic layer was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=3:1) to give the desired compound 1,1′-[(1E,3E)-2,3-diisocyano-1,3-butadiene-1,4-diyl]bis[methoxybenzene] (2.2 mg, 72%) as liver brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595415B2
Source datasetuspto-grants-2009_09
ORD IDord-3f437cc3ca224a62929b5e9b5a7990f3
Source noteuspto-grants-2009_09