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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624051Generated: November 3, 2026

Methyl iodide → 3-(2-Bromoethyl)-1-methyl-1H-indole

https://huagongshe.com/reaction/624051

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant3-(2-Bromoethyl)indoleHCID 76924—
SolventTetrahydrofuranHCID 8028—
Product3-(2-Bromoethyl)-1-methyl-1H-indoleHCID 13153306—

Reaction Steps

A flask was charged with NaH (900 mg, 37.52 mmol), MeI (3.14 mL, 50.00 mmol) and THF (7.5 mL). The resulting grey suspension was stirred at rt for 5 min, then a solution of 3-(2-bromethyl)-indol (1.12 g, 5.00 mmol) in THF (25 mL) was added dropwise. After stirring for 18 h at rt, the reaction mixture was concentrated, redissolved in DCM and washed with H2O (3×). The org. layer was dried (MgSO4), filtered and the solvent was removed under reduced pressure to yield the title compound as an yellow oil which was used as such in the next step. LC-MS conditions A: tR=0.95 min, [M+H]+=no ionization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09303023B2
Source datasetuspto-grants-2016_04
ORD IDord-798d6f26c67040a19d0eab326fdd523e
Source noteuspto-grants-2016_04