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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1600611Generated: October 29, 2026

tert-Butyl acrylate → ethyl 1-(2-tert-butoxycarbonylethyl)-4-methyl-1H-indole-2-carboxylate

https://huagongshe.com/reaction/1600611

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl acrylateHCID 15458—
ReactantBenzyltrimethylammonium hydroxideHCID 66854—
ReactantEthyl 4-methyl-1H-indole-2-carboxylateHCID 12529972—
Solvent1,4-DioxaneHCID 31275—
Productethyl 1-(2-tert-butoxycarbonylethyl)-4-methyl-1H-indole-2-carboxylateHCID 1554894487%

Reaction Conditions

Temperature61 °C

Reaction Steps

A mixture of ethyl 4-methyl-1H-indole-2-carboxylate (70.0 g, 344 mmol), tert-butyl acrylate (53.0 g, 413 mmol), benzyltrimethylammonium hydroxide (5.76 g, 34.4 mmol) and 1,4-dioxane (1,000 ml) was stirred at 60-62° C. for 8.5 hours. The solvent was distilled off under reduced pressure and water (1,000 ml) and acetic acid. (30 ml) were added to the residue, followed by extraction with ethyl acetate (twice). The extract solution was washed with a 5% aqueous sodium hydrogencarbonate solution and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the resulting residue was crystallized from isopropanol (230 ml) to obtain ethyl 1-(2-tert-butoxycarbonylethyl)-4-methyl-1H-indole-2-carboxylate (99.2 g). M.p. 78-79° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05977100
Source datasetuspto-grants-1999_11
ORD IDord-6fab74eec8664dc3abf0785da87eaa25
Source noteuspto-grants-1999_11