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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 21584Generated: October 30, 2026

1H-Indole-2-carboxylic acid, 1-methyl-5-(phenylmethoxy)-, ethyl ester → Ethyl 3-bromo-1-methyl-5-(phenylmethoxy)-1H-indole-2-carboxylate

https://huagongshe.com/reaction/21584

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Indole-2-carboxylic acid, 1-methyl-5-(phenylmethoxy)-, ethyl esterHCID 11483680—
SolventPyridineHCID 1049—
ProductEthyl 3-bromo-1-methyl-5-(phenylmethoxy)-1H-indole-2-carboxylateHCID 1536623776%

Reaction Steps

A solution of ethyl 1-methyl-5-(phenylmethoxy)-1H-indole-2-carboxylate (60.9 g, 197 mmol; Monge Vega A, et al., An. Ouim. 1976;72:267) in 550 mL of pyridine is cooled in ice and treated dropwise with a solution of pyridinium bromide perbromide (67.0 g, 209 mmol) in 200 mL of pyridine. The cooling bath is removed, and the mixture is stirred for 16 hours, then added to 4.0 L of cold water. The precipitated solid is filtered, washed with water, and recrystallized from ethyl acetate-hexane to give 58.4 g (76%) of product; mp 125-127° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05424329
Source datasetuspto-grants-1995_06
ORD IDord-4d6bfc25f1c240d4afa3ad89347851df
Source noteuspto-grants-1995_06