Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 543352Generated: October 30, 2026

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

https://huagongshe.com/reaction/543352

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 numberUS04661605
Source datasetuspto-grants-1987_04
ORD IDord-206f0e456ad34c25a7d1ef80cc621a3e
Source noteuspto-grants-1987_04