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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2361896Generated: October 26, 2026

Cyclohexanol → 1h-Indole-1-carboxylic acid,5-[(cyclohexyloxy)methyl]-,1,1-dimethylethyl ester

https://huagongshe.com/reaction/2361896

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanolHCID 7966—
Reactanttert-Butyl 5-(chloromethyl)-1H-indole-1-carboxylateHCID 66891608—
SolventDiethyl EtherHCID 3283—
Product1h-Indole-1-carboxylic acid,5-[(cyclohexyloxy)methyl]-,1,1-dimethylethyl esterHCID 2314794528%

Reaction Conditions

Temperature35 °C

Reaction Steps

A mixture of 5-chloromethyl-indole-1-carboxylic acid tert-butyl ester (0.41 g, 1.55 mmol, 1.0 eq.), cyclohexanol (0.82 mL, 5.0 eq.) and Ag2O (1.80 g, 5.0 eq.) in diethyl ether (5 mL) was stirred at 35° C. over weekend. After cooling to room temperature, the reaction mixture was filtered through celite washing with ether. The filtrate was concentrated and the residue was purified by chromatography (3% EtOAc/hexanes) to give N-Boc-5-cyclohexyloxymethylindole (160 mg, 28%) as colorless oil. 1HNMR confirmed the compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691814B2
Source datasetuspto-grants-2014_04
ORD IDord-f075611821b54be785f954d0fa043f31
Source noteuspto-grants-2014_04