4-Nitrobenzaldehyde → HCID 53810778, compound

HRID 2293764Notes

Reaction equation

HRID 2293764 reaction equation
[N+:1]([C:4]1[CH:11]=[CH:10][C:7]([CH:8]=O)=[CH:6][CH:5]=1)([O-:3])=[O:2].[N:12]([CH2:15][C:16]([O:18][CH3:19])=[O:17])=[N+:13]=[N-:14]>>[N+:1]([C:4]1[CH:11]=[CH:10][C:7]([CH:8]=[C:15]([N:12]=[N+:13]=[N-:14])[C:16]([O:18][CH3:19])=[O:17])=[CH:6][CH:5]=1)([O-:3])=[O:2]

Participants

3

Reactant 2

HCID 5414-NitrobenzaldehydeHCID 4020482Methyl 2-azidoacetate

Product 1

HCID 53810778HCID 53810778, compound

Procedure

Following the general procedure of PREPARATION 57 and making non-critical variations but starting with p-nitrobenzaldehyde (10 g) and methyl azidoacetate (30.4 g), the title compound is obtained, NMR 8.34, 8.07, 7.02, and 4.07 δ.

Workup

  1. customthe general procedure of PREPARATION 57

Sources & evidence

ORD record
ord-0313f6154fd941d7acfd2f10a178ffe6
Source dataset
uspto-grants-1997_11
Patent number
US05686610

Reaction notes

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