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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364965Generated: October 31, 2026

Methyl 3-cyclohexyl-1H-indole-6-carboxylate → Methyl 2-bromo-3-cyclohexyl-1H-indole-6-carboxylate

https://huagongshe.com/reaction/1364965

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-cyclohexyl-1H-indole-6-carboxylateHCID 11230631—
SolventChloroformHCID 6212—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-bromo-3-cyclohexyl-1H-indole-6-carboxylateHCID 1117507685%

Reaction Conditions

Temperature0 °C

Reaction Steps

Adapting the procedure of L. Chu (Tet. Lett. 1997, 38, 3871) methyl 3-cyclohexyl-6-indole carboxylate (4.65 g, 18.07 mmol) was dissolved in a mixture of THF (80 mL) and CHCl3 (80 mL). The solution was cooled in an ice bath and pyridinium bromide perbromide (pyridine tribromide, 7.22 g, 22.6 mmol, 1.25 equivalent) was added. After stirring for 1.5 h at 0° C., the reaction was judged complete by TLC. It was diluted with CHCl3 (200 mL), washed with 1M NaHSO3 (2×50 mL), saturated aqueous NaHCO3 (2×50 mL) and brine (50 mL). After drying over Na2SO4, the solvent was removed under reduced pressure and the residue crystallized from TBME-hexane. The desired 2-bromoindole derivative was collected by filtration, washed with hexane and dried (3.45 g). Evaporation of mother liquors gave a red solid that was purified by flash chromatography using 15% EtOAc in hexane yielding an additional 3.62 g of pure material. Total yield was 5.17 g (85% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888363B2
Source datasetuspto-grants-2011_02
ORD IDord-9ac2b0f5cdfd4957b6f1507f3ca0caea
Source noteuspto-grants-2011_02