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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 863299Generated: October 29, 2026

Ethyl Indole-3-carboxylate → 1-tert-Butyl 3-ethyl 1H-indole-1,3-dicarboxylate

https://huagongshe.com/reaction/863299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl Indole-3-carboxylateHCID 247965—
ReactantCarbonic acid, bis(1,1-dimethylethyl) esterHCID 10219638—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product1-tert-Butyl 3-ethyl 1H-indole-1,3-dicarboxylateHCID 53983345105.9%

Reaction Steps

A solution of 3.15 g of ethyl indole-3-carboxylate, 4.36 g of di-tert-butylcarbonate and 0.02 g of 4-DMAP in 30 ml of acetonitrile is stirred at room temperature for 15 min. The reaction mixture is then diluted with 200 ml of ethyl acetate. The organic phase is washed with dilute hydrochloric acid, water and saturated sodium chloride solution in succession, dried over sodium sulfate and concentrated. Purification by means of FC over 80 g of silica gel with a 15:1 mixture of hexane and ethyl acetate as the mobile phase gives 5.1 g of the title compound: Rf (G)=0.41.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05719141
Source datasetuspto-grants-1998_02
ORD IDord-cefa6350b4114ac1b007557d7d94c5d9
Source noteuspto-grants-1998_02