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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 903950Generated: October 30, 2026

Methyl iodide → HCID 23458318, compound

https://huagongshe.com/reaction/903950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 15572607HCID 15572607—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 23458318HCID 2345831869%

Reaction Steps

b 2.69 g of 2-hydroxy-3-phenyl-3-(2-methoxy-phenoxy)-propionitrile dissolved in 25 ml of anhydrous DMF and 7.1 g of methyl iodide were stirred at 0° C. Addition was made, in portions, of 2.18 g of 55% NaH. After the addition, the whole was stirred at 0°-5° C. for 1 and a half hours. Under an atmosphere of nitrogen the whole was then decomposed cautiously with water, diluted with plentiful water, extracted with ethyl acetate and washed with water. The organic phase was dried over Na2SO4 and evaporated to dryness, in this way obtaining 1.95 g of 2-methoxy-3-phenyl-3-(2-methoxy-phenoxy)-propionitrile as an oil. Yield=69%. Analogously, all the 2-methoxy-propionitrile derivatives useful for the preparation of the 2-methoxy-propylamines listed in example 2 and obtained according to the reduction of Example 3, were prepared.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04229449
Source datasetuspto-grants-1980_10
ORD IDord-c814aa9e8f4f406787d3c80ae2ffc61c
Source noteuspto-grants-1980_10