Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 511849Generated: October 26, 2026

Indole → ethyl trans-2-((1H-indol-1-yl)methyl)cyclopropanecarboxylate

https://huagongshe.com/reaction/511849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 2-(((methylsulfonyl)oxy)methyl)cyclopropanecarboxylateHCID 57184993—
SolventDimethylformamideHCID 6228—
Productethyl trans-2-((1H-indol-1-yl)methyl)cyclopropanecarboxylateHCID 6729069954%

Reaction Steps

To a suspension of sodium hydride (60%, 55 mg, 1.4 mmol) in DMF (5 mL) was added indole (135 mg, 1.2 mmol). After stirring at room temperature for 10 min, ethyl 2-(((methylsulfonyl)oxy)methyl)cyclopropanecarboxylate (307 mg, 1.4 mmol) was added. After stirring at room temperature for 6 h, the mixture was poured into water, and the aqueous layer was extracted with EtOAc twice. The combined organic layer was dried over sodium sulfate and concentrated in vacuo. The residue was purified by column chromatography on silica gel eluting with hexane/ethyl acetate (10:1-5:1) to give 153 mg (54%) of the title compound as a pale brown oil;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09101616B2
Source datasetuspto-grants-2015_08
ORD IDord-0f75e6b3148947f98c16685a91637156
Source noteuspto-grants-2015_08