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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1481774Generated: October 31, 2026

Potassium tert-butoxide → tert-butyl 2,4-di-tert-butoxy-6-(1-methyl-1H-indol-5-yl)-5-vinylnicotinate

https://huagongshe.com/reaction/1481774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
Reactanttert-butyl 2,4-difluoro-6-(1-methyl-1H-indol-5-yl)-5-vinylnicotinateHCID 89422971—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl 2,4-di-tert-butoxy-6-(1-methyl-1H-indol-5-yl)-5-vinylnicotinateHCID 89422958196.4%

Reaction Steps

Into a solution of tert-butyl 2,4-difluoro-6-(1-methyl-1H-indol-5-yl)-5-vinylnicotinate (72 mg, 0.2 mmol) in THF (1.0 mL) at −78° C. was added a solution of potassium tert-butoxide (1.0 M×0.48 mL, 0.48 mmol). The temperature was allowed to rise to room temperature and the reaction was quenched with saturated NH4Cl. The mixture was extracted with ethyl acetate. The organic layers were combined, dried, evaporated and purified by silica chromatography (0-10% ethyl acetate in hexanes) to give tert-butyl 2,4-di-tert-butoxy-6-(1-methyl-1H-indol-5-yl)-5-vinylnicotinate (94 mg, 47%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409905B2
Source datasetuspto-grants-2016_08
ORD IDord-e891cadbc2494f96984e14c8d797fb89
Source noteuspto-grants-2016_08