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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49055Generated: October 27, 2026

Water → 5-(2-tert-butoxycarbonyl-vinyl)-1H-indole-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/49055

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl acrylateHCID 15458—
ReactantEthyl 5-Bromoindole-2-carboxylateHCID 259091—
CatalystHCID 178418476HCID 178418476—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
Product5-(2-tert-butoxycarbonyl-vinyl)-1H-indole-2-carboxylic acid ethyl esterHCID 6958712628.5%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 5-bromoindole-2-carboxylic acid ethyl ester (2.68 g, 10 mmol), tert-butyl acrylate (4.4 mL, 30 mmol) and dichlorobis(triphenylphosphine)palladium(II) (0.7 g, 1 mmol) and triethylamine (17 mL) in acetic acid (17 mL) was heated at 120° C. in a closed vessel for 6 hrs. The cooled reaction mixture was poured into water and dichloromethane. The biphasic mixture was filtered through a pad of celite and the aqueous layer was extracted with dichloromethane (2×). The combined organic layers were washed with saturated sodium bicarbonate solution, brine, dried and concentrated. The residue was purified by column chromatography (10% of ethyl acetate in hexanes) to give 900 mg (28%) of 5-(2-tert-butoxycarbonyl-vinyl)-1H-indole-2-carboxylic acid ethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706709B2
Source datasetuspto-grants-2004_03
ORD IDord-9653ef1145b4482bb4edf3f452aeadc5
Source noteuspto-grants-2004_03