4-(2-Bromoethoxy)Benzaldehyde → HCID 15490947, compound

HRID 1418986Notes

Reaction equation

HRID 1418986 reaction equation
[CH3:1][C:2]1[NH:3][C:4](=[O:9])[CH:5]=[C:6]([CH3:8])[N:7]=1.Br[CH2:11][CH2:12][O:13][C:14]1[CH:21]=[CH:20][C:17]([CH:18]=[O:19])=[CH:16][CH:15]=1>>[CH3:1][C:2]1[N:3]([CH2:11][CH2:12][O:13][C:14]2[CH:21]=[CH:20][C:17]([CH:18]=[O:19])=[CH:16][CH:15]=2)[C:4](=[O:9])[CH:5]=[C:6]([CH3:8])[N:7]=1

Participants

3

Reactant 2

HCID 2627064-(2-Bromoethoxy)BenzaldehydeHCID 1354086402,6-Dimethyl-1H-pyrimidin-4-one

Product 1

HCID 15490947HCID 15490947, compoundYield 30%

Procedure

The title compound (0.8 g, 30%) was prepared from 2,4-dimethyl-1,6-dihydro-6-pyrimidone (1.3 g, 10.48 mmol) and 4-[2-bromoethoxy]benzaldehyde (2.4 g, 10.48 mmol) in the presence of a base K2C3 (2.89 g, 20.96 mmol) by a similar procedure as described in preparation 1.

Workup

  1. customas described in preparation 1

Sources & evidence

ORD record
ord-3bd5fc7ebd29446fbbd74fd1fe80ce4a
Source dataset
uspto-grants-1999_03
Patent number
US05885997

Reaction notes

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