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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253065Generated: November 1, 2026

Iodoethane → HCID 14096505, compound

https://huagongshe.com/reaction/1253065

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantPotassium HydroxideHCID 14797—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178418505HCID 178418505—
SolventDimethylformamideHCID 6228—
ProductHCID 14096505HCID 14096505—

Reaction Steps

To a suspension of 3,4-dihydro-6-(3,4-dimethoxyphenyl)-3-methyl-4-(2,4,6-trimethylphenylimino)-2-(1H)pyrimidone (14.2 g) in N,N-dimethylformamide (1.42 ml) were added potassium hydroxide (5.5 g) and ethyl iodide (6.0 ml) and the mixture was stirred at ambient temperature for 2.5 hours. To the reaction mixture were added additional potassium tert-butoxide (5.0 g) and ethyl iodide (3.0 ml) and the mixture was stirred at ambient temperature for more 2 hours. The mixture was poured into ice-water (150 ml). The resulting precipitates were collected by filtration, air-dried and subjected to column chromatography on silica gel using a mixture of dichloromethane and methanol as an eluent to give 3,4-dihydro-6-(3,4-dimethoxyphenyl)-2-ethoxy-3-methyl-4-(2,4,6-trimethylphenylimino)pyrimidine (0.135 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04746664
Source datasetuspto-grants-1988_05
ORD IDord-ae31184430a1402db4637e355ab0f72d
Source noteuspto-grants-1988_05