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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219138Generated: October 26, 2026

Methyl iodide → Methyl 2-(quinolin-6-YL)propanoate

https://huagongshe.com/reaction/219138

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantMethyl 6-quinolineacetateHCID 1514202—
ReactantLithium HexamethyldisilazideHCID 2733832—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-(quinolin-6-YL)propanoateHCID 5769120085%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a 250 ml round-bottomed flask was added lithium bis(trimethylsilyl)amide (2.0 g, 12 mmol) and tetrahydrofuran (75 ml). The mixture was cooled to −78° C. and methyl 2-(quinolin-6-yl)acetate (2.0 g, 9.9 mmol) was added as a solution in 1 ml THF. This was stirred at −78° C. for 30 min and then methyl iodide (0.75 ml, 12 mmol) was added. This was stirred for 30 min at −78° C. and then allowed to warm to rt. The mixture was quenched with sat NH4Cl (40 mL) and diluted with water (200 mL). The mixture was concentrated in vacuo to remove the THF and then was extracted with EtOAc (2×100 ml). The combined extracts were washed with brine (50 ml), dried (Na2SO4) and concentrated onto silica. Purification by silica gel chromatography (20 to 60% EtOAc/hexane) afforded the title compound as a brown oil (1.8 g, 85%). MS (ESI, pos. ion) m/z: 216 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198448B2
Source datasetuspto-grants-2012_06
ORD IDord-29a1b68a8c9f4cd88fae5ae687d17c18
Source noteuspto-grants-2012_06