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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 976583Generated: October 29, 2026

Bromide ion → HCID 21468933, compound

https://huagongshe.com/reaction/976583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantHCID 21468934HCID 21468934—
ReactantHCID 21468958HCID 21468958—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21468933HCID 2146893335.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

Sodium bis(trimethylsilyl)amide (5.6 ml of 1M solution in THF) in 40 ml THF was added dropwise at 0° C. to a solution of 5-(2-cyanophenyl)indole (5.04 mmoles, 1.1 g) in 100 ml THF and stirred at 0° C. for 30 minutes. Methyl 3-bromononanoate (5.6 mmoles, 1.32 g) in 20 ml THF was added dropwise. The reaction was stirred at room temperature for 12 hours. An additional 5 mmoles of the base and the bromide were added. The reaction was stirred an additional 12 hours, added to ice water and extracted into ethyl acetate. The organic phase was dried over sodium sulfate and concentrated. The intermediate was chromatographed over silica gel eluted with 50% ether in hexane to yield 700 mg of methyl 3-[5-(2-cyanophenyl)indol-1-yl]nonanoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05612360
Source datasetuspto-grants-1997_03
ORD IDord-1f0547f4d35c461ca4a547b0409f2028
Source noteuspto-grants-1997_03