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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2361895Generated: October 26, 2026

Potassium Carbonate → 1h-Indole-1-carboxylic acid,5-[(cyclohexylthio)methyl]-,1,1-dimethylethyl ester

https://huagongshe.com/reaction/2361895

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantCyclohexanethiolHCID 15290—
Reactanttert-Butyl 5-(chloromethyl)-1H-indole-1-carboxylateHCID 66891608—
SolventDimethylformamideHCID 6228—
SolventAmmonium ChlorideHCID 25517—
Product1h-Indole-1-carboxylic acid,5-[(cyclohexylthio)methyl]-,1,1-dimethylethyl esterHCID 6689203174%

Reaction Conditions

Temperature40 °C

Reaction Steps

A mixture of 5-chloromethyl-indole-1-carboxylic acid tert-butyl ester (0.82 g, 3.10 mmol, 1.0 eq.), cyclohexyl mercaptan (0.53 mL, 1.4 eq.) and K2CO3 (0.90 g, 2.0 eq.) in DMF (6 mL) was heated at 40° C. until reaction completed. The reaction mixture was cooled to room temperature, diluted with sat. NH4Cl and extracted with diethyl ether. The organic extracts were dried over MgSO4, filtered and concentrated. The resulting mixture was purified by chromatography (5% EtOAc/hexanes) to give 5-cyclohexylsulfanylmethyl-indole-1-carboxylic acid tert-butyl ester (0.79 g, 74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691814B2
Source datasetuspto-grants-2014_04
ORD IDord-65927ada2b5a42ca85eaa53180e92b1e
Source noteuspto-grants-2014_04