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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 621527Generated: November 2, 2026

Iodoethane → HCID 14096505, compound

https://huagongshe.com/reaction/621527

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 numberUS04824851
Source datasetuspto-grants-1989_04
ORD IDord-7ac359ad5bce400d859ac576a10336d4
Source noteuspto-grants-1989_04