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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857274Generated: October 31, 2026

Methyl iodide → Quinoline

https://huagongshe.com/reaction/857274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant6-(Methylsulfonylmethyl)-8-bromoquinolineHCID 9879373—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
SolventAmmonium ChlorideHCID 25517—
ProductQuinolineHCID 7047—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of the 8-bromo-6-methanesulfonylmethyl-quinoline (1.0 eq) from Step 1 in THF (0.1M) at 0° C., was added potassium t-butoxide (1.3 eq; 1M in THF) over 30 min. After 0.5 h at 0° C., MeI (1.6 eq) was added and the resulting reaction mixture was stirred at 0° C. for 2 h. A second portion of potassium t-butoxide (1.0 eq; 1M in THF) was added over 30 min, followed by MeI (1.6 eq). The mixture was stirred at room temperature for 2 h. The mixture was poured in saturated aqueous NH4Cl and extracted with EtOAc (2×). The combined organic extracts were washed with brine, dried over MgSO4, filtered and concentrated. The residue was vigorously stirred in Et2O and the title compound was isolated by filtration as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07144896B2
Source datasetuspto-grants-2006_12
ORD IDord-c2d766fd091547e39b968cb85319b13e
Source noteuspto-grants-2006_12