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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 725827Generated: October 31, 2026

Dichloromethane → HCID 70205439, compound

https://huagongshe.com/reaction/725827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantBenzoyl chloride, 3,4,5-trimethoxy-HCID 78282—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 22372113HCID 22372113—
SolventPyridineHCID 1049—
ProductHCID 70205439HCID 7020543964.2%

Reaction Steps

A dry dichloromethane solution (5 ml) containing 650 mg of 3,4,5-trimethoxybenzoyl chloride was slowly added dropwise to 5 ml of a pyridine solution containing 520 mg of the crystals obtained in step (7), and stirred at room temperature for 2 hours. After completion of the reaction, a saturated aqueous NaHCO3 solution was added and the reaction mixture was extracted with dichloromethane. The organic layer was collected and washed with a 1N aqueous hydrochloric acid until the pH of the water layer became about 1. The organic layer was allowed to stand for 2 hours, washed with water and a saturated saline solution, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was recrystallized from dichloromethane-n-hexane to provide 480 mg of the object compound as colorless crystals. Table 2 shows the structure and melting point of the compound obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05707997
Source datasetuspto-grants-1998_01
ORD IDord-e99838202452442f8acbd640deded043
Source noteuspto-grants-1998_01