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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789276Generated: October 31, 2026

Methanol → 3-Methoxy-3-(1-ethyl-2-methylindol-3-yl)phthalide

https://huagongshe.com/reaction/1789276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPyridineHCID 1049—
ReactantThionyl ChlorideHCID 24386—
ReactantBenzoic acid, 2-[(1-ethyl-2-methyl-1H-indol-3-yl)carbonyl]-HCID 3084978—
Solvent1,2-DichloroethaneHCID 11—
Product3-Methoxy-3-(1-ethyl-2-methylindol-3-yl)phthalideHCID 13931503—

Reaction Steps

Proceeding in a manner similar to that described in Example 1 above, 5.1 g of 2-(1-ethyl-2-methylindol-3-yl)carbonylbenzoic acid, 1.2 ml of thionyl chloride and 5.0 ml of methyl alcohol were interacted in 30.0 ml of ethylene dichloride in the presence of 1.3 ml of pyridine to obtain 2.1 g of 3-methoxy-3-(1-ethyl-2-methylindol-3-yl)phthalide (Formula III: R0 =R=R1 =R2 =R8 =H; R6 =C2H5 ; R7 =Y=CH3 ; X=O), a dark brown-colored oil. Significant infrared maxima appeared at 1770 (C=O; s) and 740 cm-1 (C=O; s). Analysis by mass spectrum showed m/e peaks at 321 (M+) and 290 (M+ -OCH3). A toluene solution of the product spotted on an acidic clay-coated paper developed a red-purple-colored image.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04688059
Source datasetuspto-grants-1987_08
ORD IDord-e9cef888cfe447b9a68601f054b7153b
Source noteuspto-grants-1987_08