Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 381327Generated: October 31, 2026

Acetate → 2-(1,3-benzodioxol-5-yl)-2-(5-bromo-1-methyl-1H-3-indolyl)acetic acid

https://huagongshe.com/reaction/381327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetateHCID 175—
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 2-(1,3-benzodioxol-5-yl)-2-(5-bromo-1-methyl-1H-3-indolyl)acetateHCID 22467212—
Solvent1,4-DioxaneHCID 31275—
Product2-(1,3-benzodioxol-5-yl)-2-(5-bromo-1-methyl-1H-3-indolyl)acetic acidHCID 2246726183.6%

Reaction Steps

Aqueous sodium hydroxide (14.7 ml of 1M) was added to a solution of methyl 2-(1,3-benzodioxol-5-yl)-2-5-bromo-1-methyl-1H-3-indolyl) acetate from (b) (1.97 g, 4.9 mmol) in a 3:1 mixture of methanol and 1,4-dioxane at ambient temperature. The mixture was heated to reflux for 1 hour before recooling and removing the organic solvents in vacuo. The residue was redissolved in water and acidified with drops of concentrated hydrochloric acid. The resultant precipitate was extracted with diethylether, dried (magnesium sulphate) and the solvent removed in vacuo. The residue was crystallised from diisopropylether to give the subtitle compound (1.59 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06306852B1
Source datasetuspto-grants-2001_10
ORD IDord-4f8514152ff447b0bc6406ae9e1e6b02
Source noteuspto-grants-2001_10