Pyridine → HCID 86748831, compound

HRID 1755706Notes

Reaction equation

HRID 1755706 reaction equation
[Br:1][CH2:2][C:3]([O:5][CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)=[O:4].[N:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>>[Br-:1].[C:3]([O-:5])(=[O:4])[CH3:2].[CH2:6]([N+:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[C:7]1[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=1.[CH2:6]([N+:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[C:7]1[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=1

Participants

3

Reactant 2

HCID 1049PyridineHCID 62576Benzyl bromoacetate

Product 1

HCID 86748831HCID 86748831, compoundYield 80%

Procedure

The title compound was prepared as described in Example 1 from pyridine and benzyl bromoacetate in a yield of 80%.

Sources & evidence

ORD record
ord-435bfd5f756145ac8daf81d8b2c2b080
Source dataset
uspto-grants-1995_08
Patent number
US05438140

Reaction notes

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