Pyridine →

HRID 1755708Notes

Reaction equation

[Cl:1][CH2:2][C:3](=[O:11])[CH2:4][C:5]([O:7]C(C)C)=[O:6].[N:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>>[Cl-:1].[C:5]([O-:7])(=[O:6])[CH2:4][C:3]([CH3:2])=[O:11].[CH:3]([C:13]1[CH:14]=[CH2+:15][CH:16]=[CH:17][N:12]=1)([CH3:4])[CH3:2].[CH:3]([C:13]1[CH:14]=[CH2+:15][CH:16]=[CH:17][N:12]=1)([CH3:4])[CH3:2]

Participants

Reactant 2

HCID 1049Pyridine

HCID 2795580Isopropyl 4-chloroacetoacetate

Product 0

No Product data yet.

Procedure

The title compound was prepared as described in Example 1 from pyridine and isopropyl 4-chloroacetoacetate in a yield of 71%.

Sources & evidence

ORD record: ord-7a5fbb9fb88c4614a2214676fb64ef00
Source dataset: uspto-grants-1995_08
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05438140

Reaction notes

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