Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1891017Generated: October 30, 2026

Tetrabutylammonium Fluoride → Methyl 6-chloro-1H-indole-5-carboxylate

https://huagongshe.com/reaction/1891017

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantMethyl 4-(acetylamino)-2-chloro-5-[(trimethylsilyl)ethynyl]benzoateHCID 11839199—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 6-chloro-1H-indole-5-carboxylateHCID 1072713286%

Reaction Steps

A solution of methyl-2-chloro-4-acetamido-5-(2-trimethylsilylethynyl)-benzoate (1.9 g, 5.9 mmol) in THF (15.0 mL) containing tetrabutyl ammonium fluoride (1.9 g, 6.0 mmol) was heated to reflux for 6 h under nitrogen. The reaction mixture was concentrated to dryness and the residue partitioned between ethyl acetate (25 mL) and water (25 mL). The organic layer was washed with water, dried (MgSO4) and concentrated to dryness. The residue was purified by silica gel flash chromatography using 25% ethyl acetate in heptane to afford the title compound as a light brown powder (0.98 g, 86%), m/z 210 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507499B2
Source datasetuspto-grants-2013_08
ORD IDord-21b2da86f2cd45298935188e6bc2caf6
Source noteuspto-grants-2013_08