Methanol → (4-Nitro-1,2-phenylene)dimethanol

HRID 552554Notes

Reaction equation

HRID 552554 reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([C:13](O)=[O:14])[C:7](=[CH:11][CH:12]=1)[C:8](O)=[O:9])([O-:3])=[O:2].CO>C1COCC1>[N+:1]([C:4]1[CH:12]=[CH:11][C:7]([CH2:8][OH:9])=[C:6]([CH2:13][OH:14])[CH:5]=1)([O-:3])=[O:2]

Participants

4

Procedure

A solution of 4-nitrophthalic acid (40 g, 189.5 mmol) in THF (500 mL) was added dropwise over 1.5 h to a solution of borane-THF complex (1 M, 490 mL, 490 mmol), keeping the reaction temperature between 0° C. and 5° C. After the addition, the reaction mixture was allowed to warm slowly to ambient temperature and stirred for 18 h. MeOH (100 mL) was added carefully and the precipitated solid dissolved. The mixture was concentrated in vacuo to about 500 mL, cooled to 0° C., and 10 N NaOH was added to adjust the pH to 10-11. This mixture was extracted with EtOAc (3×600 mL) and the combined organic layers were washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo to give the title compound. MS: m/z=207 (M-OH+CH3CN).

Workup

  1. customthe reaction temperature between 0° C. and 5° C
  2. additionAfter the addition
  3. dissolutionthe precipitated solid dissolved
  4. concentrationThe mixture was concentrated in vacuo to about 500 mL
  5. temperaturecooled to 0° C.
  6. addition10 N NaOH was added
  7. extractionThis mixture was extracted with EtOAc (3×600 mL)
  8. washthe combined organic layers were washed with brine
  9. dry with materialdried over Na2SO4
  10. filtrationfiltered
  11. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-eca77510c27941e48fec591a1967460b
Source dataset
uspto-grants-2011_05
Patent number
US07951795B2

Reaction notes

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