Bromocyclopentane → Methyl 3-cyclopentyloxy-4-nitrobenzoate

HRID 1940306Notes

Reaction equation

HRID 1940306 reaction equation
[CH:1]1(Br)[CH2:5][CH2:4][CH2:3][CH2:2]1.C(=O)([O-])[O-].[K+].[K+].[OH:13][C:14]1[CH:15]=[C:16]([CH:21]=[CH:22][C:23]=1[N+:24]([O-:26])=[O:25])[C:17]([O:19][CH3:20])=[O:18]>CN(C)C=O>[CH:1]1([O:13][C:14]2[CH:15]=[C:16]([CH:21]=[CH:22][C:23]=2[N+:24]([O-:26])=[O:25])[C:17]([O:19][CH3:20])=[O:18])[CH2:5][CH2:4][CH2:3][CH2:2]1

Participants

5

Reactant 3

HCID 8728BromocyclopentaneHCID 11430Potassium CarbonateHCID 294866Methyl 3-hydroxy-4-nitrobenzoate

Product 1

HCID 21187961Methyl 3-cyclopentyloxy-4-nitrobenzoateYield 102.2%

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

Cyclopentyl bromide (38.7 g, 0.26 mol) is added slowly (over 1 hour) to a stirred suspension of potassium carbonate (41.4 g, 0.3 mol) in N,N-dimethylformamide (200 mL) containing methyl 3-hydroxy-4-nitrobenzoate (39.4 g, 0.2 tool) at 65° C. and then the stirring is continued for 4 hours. The mixture is allowed to cool and then filtered. The flitrate is diluted with water (700 mL) containing sodium chloride (50 g) and then extracted with toluene (3×200 mL). The combined organic extract is washed with 1N sodium hydroxide solution (1×200 mL) and then water (2×200 mL) and then evaporated under reduced pressure to give methyl 3-cyclopentyloxy-4-nitrobenzoate (54.2 g, 100%) as a pale green solid which is used without further purification.

Workup

  1. temperatureto cool
  2. filtrationfiltered
  3. additionThe flitrate is diluted with water (700 mL)
  4. additioncontaining sodium chloride (50 g)
  5. extractionextracted with toluene (3×200 mL)
  6. extractionThe combined organic extract
  7. washis washed with 1N sodium hydroxide solution (1×200 mL)
  8. customwater (2×200 mL) and then evaporated under reduced pressure

Sources & evidence

ORD record
ord-d3030c42f1554c66ad60990f5658fb82
Source dataset
uspto-grants-1997_12
Patent number
US05698711

Reaction notes

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