Pyridine → HCID 19432280, compound

HRID 1736262Notes

Reaction equation

HRID 1736262 reaction equation
[C:1]([C:5]1[CH:14]=[CH:13][C:8]([C:9](=[O:12])[CH2:10][Cl:11])=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].[N:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>>[Cl-:11].[C:1]([C:5]1[CH:14]=[CH:13][C:8]([C:9](=[O:12])[CH2:10][N+:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2]

Participants

3

Reactant 2

HCID 1049PyridineHCID 2296611-(4-Tert-butylphenyl)-2-chloroethan-1-one

Product 1

HCID 19432280HCID 19432280, compoundYield 94%

Procedure

The title compound was prepared similarly to Example 1 from 4-tert-butylphenacyl chloride and pyridine in a yield of 94%.

Sources & evidence

ORD record
ord-d3f6177523434296822e1b195943ff8a
Source dataset
uspto-grants-1996_07
Patent number
US05541032

Reaction notes

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