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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789272Generated: October 26, 2026

Pyridine → 3-[3,4-dichloro-2(5H)-furanon-5-yl]oxy-3-(2-methyl-4-diethylaminophenyl)phthalide

https://huagongshe.com/reaction/1789272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantThionyl ChlorideHCID 24386—
Reactant2-(4-(Diethylamino)-2-methylbenzoyl)benzoic acidHCID 104335—
ReactantMucochloric AcidHCID 2771871—
Solvent1,2-DichloroethaneHCID 11—
Product3-[3,4-dichloro-2(5H)-furanon-5-yl]oxy-3-(2-methyl-4-diethylaminophenyl)phthalideHCID 1393150184.2%

Reaction Steps

In a manner similar to that described in Example 1 above, 2.0 g of 2-(2-methyl-4-diethylaminophenyl)carbonylbenzoic acid, 0.77 g of thionyl chloride and 1.1 g of mucochloric acid were interacted in 20.0 ml of ethylene dichloride in the presence of 0.8 ml of pyridine to obtain 2.5 g of 3-[3,4-dichloro-2(5H)-furanon-5-yl]oxy-3-(2-methyl-4-diethylaminophenyl)phthalide (Formula II: R0 =R=R1 =R2 =H; R4 =R4' =R5 =CH3 ; X=O; Y=3,4-dichloro-2-(5H)-furanon-5-yl), an orange-colored oil. A significant infrared maximum appeared at 1758 cm-1 (C=O; s). A toluene solution of the product spotted on an acidic clay-coated paper developed a yellow-colored image.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04688059
Source datasetuspto-grants-1987_08
ORD IDord-a810024a81c5474486c77da724e3fcd8
Source noteuspto-grants-1987_08