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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712197Generated: October 29, 2026

Methyl iodide → HCID 66977074, compound

https://huagongshe.com/reaction/712197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantHexaneHCID 8058—
ReactantSodium hydrideHCID 24758—
ReactantHCID 66977004HCID 66977004—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66977074HCID 6697707432%

Reaction Steps

To an ice-cold solution of ethyl 1-(5-bromopyrimidin-2-yl)piperidine-2-carboxylate (0.37 g, 1.18 mmol) in THF (25 mL) was added NaH (60% dispersion in mineral oil, 0.06 g, 1.41 mmol) portion wise. The mixture was stirred at the same temperature for 45 min followed by addition of MeI (0.52 mL, 8.26 mmol) at 0° C. The temperature of the reaction was slowly raised up to rt and left to stir for 16 h. The reaction was then cooled to 0° C., quenched by drop wise addition of ice-cold water then extracted with EtOAc (3×100 mL). The combined organics were washed with brine, dried (Na2SO4), filtered and concentrated under reduced pressure. The crude residue was purified over 100-200 M silica-gel by using 2% EtOAc: hexane to obtain the desired product as off-white solid (0.115 g, 32% yield). MS: 300.09 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181234B2
Source datasetuspto-grants-2015_11
ORD IDord-d19fd3c1289e4f73933128d4163993d5
Source noteuspto-grants-2015_11