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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1818908Generated: October 31, 2026

Chloromethyl Methyl Ether → HCID 68898068, compound

https://huagongshe.com/reaction/1818908

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 12514007HCID 12514007—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68898068HCID 6889806840.3%

Reaction Steps

4-methyl-quinoline-3-carbonitrile (600 mg, 3.567 mmol) was dissolved in 10 mL of anhydrous THF, added with LHMDS (1M solution in THF, 3.9 mL, 3.924 mmol) at −78° C. under the nitrogen atmosphere and then stirred for about 1 hour at the same temperature. The mixture was dropwisely added with chloromethyl methyl ether (0.30 mL, 3.924 mmol) and then stirred for about 1 hour at −50° C., and then for about 1 hour at 0° C. The above mixture, while being stirred at 0° C., was added with 5 mL of a saturated solution of ammonium chloride and 10 mL of distilled water and then extracted twice with 50 mL of EtOAc. The resulting organic layer was washed with a saturated solution of sodium chloride, dried with anhydrous sodium sulfate and filtered. A silica gel column chromatography (30% EtOAc/Hexanes) was performed on the residue resulted by concentration of the above filtrate and obtained 305 mg (40%) of 4-(2-methoxy-ethyl)-quinoline-3-carbonitrile in pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601736B2
Source datasetuspto-grants-2009_10
ORD IDord-578c4388bb5345b8b30ec1c140e19289
Source noteuspto-grants-2009_10