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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434017Generated: October 31, 2026

Tributylphosphine → 5-Allyloxy-1-[(2-thiophen-3-yl)ethyl]-1h-indole-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/434017

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
ReactantThiophene-3-ethanolHCID 83731—
ReactantEthyl 5-[(prop-2-en-1-yl)oxy]-1H-indole-2-carboxylateHCID 13286893—
SolventTetrahydrofuranHCID 8028—
Product5-Allyloxy-1-[(2-thiophen-3-yl)ethyl]-1h-indole-2-carboxylic acid ethyl esterHCID 1209446594%

Reaction Steps

To solution of 5-allyloxyindole-2-carboxylic acid ethyl ester (1.0 g, 4.08 mmol) in THF (10 mL) was added azodicarboxylic acid bis[dimethylamide] (TMAD; 1.4 g, 8.15 mmol). After stirring at room temperature for 20 min, 2-(3-thienyl)ethanol (0.78 g, 6.12 mmol) was added followed by the addition of tributyl phosphine (1.65 g, 8.15 mmol). After stirring at room temperature for 18 h, the reaction was partitioned between ethyl acetate and water. The organic layer was washed with brine and dried over Na2SO4. Purification by flash colunmn chromatography (silica gel, EtOAc/hexanes) yielded the desired product as an oil (1.36 g, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06670388B1
Source datasetuspto-grants-2003_12
ORD IDord-2659ad643eac46948a902f9d8b56e9fb
Source noteuspto-grants-2003_12