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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 743888Generated: November 1, 2026

Bromide ion → HCID 21468933, compound

https://huagongshe.com/reaction/743888

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 3bromononanoate (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 numberUS05556981
Source datasetuspto-grants-1996_09
ORD IDord-b21a37faff41432fb747c841349c5e3e
Source noteuspto-grants-1996_09