Morpholine → Methyl 5-(morpholin-4-yl)-2-nitrobenzoate

HRID 1656923Notes

Reaction equation

HRID 1656923 reaction equation
Cl[C:2]1[CH:3]=[CH:4][C:5]([N+:12]([O-:14])=[O:13])=[C:6]([CH:11]=1)[C:7]([O:9][CH3:10])=[O:8].[NH:15]1[CH2:20][CH2:19][O:18][CH2:17][CH2:16]1>CN(C=O)C.CO>[N:15]1([C:2]2[CH:3]=[CH:4][C:5]([N+:12]([O-:14])=[O:13])=[C:6]([CH:11]=2)[C:7]([O:9][CH3:10])=[O:8])[CH2:20][CH2:19][O:18][CH2:17][CH2:16]1

Participants

5

Reactant 2

HCID 8083MorpholineHCID 171018Methyl 5-chloro-2-nitrobenzoate

Product 1

HCID 14983554Methyl 5-(morpholin-4-yl)-2-nitrobenzoate

Reagents, catalysts & solvents 2

HCID 887MethanolSolventHCID 6228DimethylformamideSolvent2×

Procedure

A solution of 2.0 g (9.28 mmol) product from Step A and 1.6 mL (18.6 mmol) morpholine in 20 mL DMF was heated to 90° C. for 6 hours. After the mixture had cooled to room temperature, the DMF was stripped off in vacuo. The crude material was then redissolved in methanol and stirred with 20 g Amberlyst-A26® for about 20 minutes. The mixture was then stripped of solvent and used without further purification in the next step. Rf 0.20 in 40% EtOAc/hexane, visualized by UV and visible light.

Workup

  1. customused without further purification in the next step

Sources & evidence

ORD record
ord-05a6edecce864bc6af99db704f310bad
Source dataset
uspto-grants-1993_10
Patent number
US05256667

Reaction notes

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