Sulfuric Acid → 2-Nitro-6-n-propylphenol

HRID 1385409

Reaction equation

HRID 1385409 reaction equation
[CH2:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[OH:10])[CH2:2][CH3:3].[N+:11]([O-])([O-:13])=[O:12].[Na+].S(=O)(=O)(O)O.N([O-])=O.[Na+]>C(Cl)Cl>[N+:11]([C:6]1[CH:7]=[CH:8][CH:9]=[C:4]([CH2:1][CH2:2][CH3:3])[C:5]=1[OH:10])([O-:13])=[O:12]

Participants

6

Reactant 4

HCID 1118Sulfuric AcidHCID 125702-PropylphenolHCID 24268Sodium NitrateHCID 23668193Sodium Nitrite

Product 1

HCID 150363142-Nitro-6-n-propylphenolYield 48%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent2×

Procedure

2-n-propylphenol (5.00 g, 36.8 mmol) was dissolved in methylene chloride (40 mL) followed by the addition of sodium nitrate (3.43 g, 40.5 mmol). The addition of sulfuric acid (45 mL/3M) was then made, followed by addition of a catalytic amount of sodium nitrite. The mixture was allowed to stir. After 24 hours, the reaction mixture was diluted with methylene chloride and extracted with water. The organic layer was dried over MgSO4 and filtered. The solvent was evaporated and chromatography of the resulting solid on silica gel (4%MeOH/CH2C]2) gave the desired product (3.2 mg, 48%). 1H NMR (CD3COCD3): d 7.99 (d, 1H), 7.46 dd, 1H), 6.90 (t, 1H), 2.70 (t, 2H), 1.70 (m, 2H), 1.00 (t, 3H).

Workup

  1. extractionextracted with water
  2. dry with materialThe organic layer was dried over MgSO4
  3. filtrationfiltered
  4. customThe solvent was evaporated

Sources & evidence

ORD record
ord-6a7f03e5a8884a56b5d30b389fb343d7
Source dataset
uspto-grants-2001_07
Patent number
US06262113B1

Linked notes

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