Sulfuric Acid → (3-Iodo-2-methylphenyl)methanol

HRID 1995119Notes

Reaction equation

HRID 1995119 reaction equation
Cl.[OH:2][CH2:3][C:4]1[C:5]([CH3:11])=[C:6]([CH:8]=[CH:9][CH:10]=1)N.S(=O)(=O)(O)O.[N+]([O-])([O-])=O.[Na+].[I-:22].[K+]>O.[Cu]>[I:22][C:6]1[C:5]([CH3:11])=[C:4]([CH:10]=[CH:9][CH:8]=1)[CH2:3][OH:2]

Participants

7

Procedure

A stirred solution of 3-hydroxymethyl-2-methylaniline hydrochloride (43.4 g, 0.25 mole) and 17.2 ml of concentrated sulfuric acid in ice-water was cooled to 0°, and a solution of sodium nitrate (17.3 g, 0.25 mole) in water was added dropwise. Upon complete addition, the reaction mixture was stirred for an additional 0.5 hour, then an additional 8 ml of concentrated sulfuric acid was added dropwise. With the temperature maintained at 0°, a solution of potassium iodide (49.8 g, 0.30 mole) in water was added dropwise to the reaction mixture, followed by the addition of 0.1 gram of copper powder. The reaction mixture was slowly warmed to 70° where it stirred for 1 hour. The reaction mixture was then allowed to stand for 18 hours while cooling to room temperature. The reaction mixture was then taken up in water and extracted with chloroform. The chloroform extract was washed with an aqueous saturated solution of sodium bisulfite, then with water. The chloroform layer was dried and filtered. The filtrate was evaporated under reduced pressure to give 3-iodo-2-methylbenzyl alcohol (15.2 g) as a dark solid.

Workup

  1. additionUpon complete addition
  2. temperatureWith the temperature maintained at 0°
  3. temperatureThe reaction mixture was slowly warmed to 70° where it
  4. stirringstirred for 1 hour
  5. waitto stand for 18 hours
  6. extractionextracted with chloroform
  7. extractionThe chloroform extract
  8. washwas washed with an aqueous saturated solution of sodium bisulfite
  9. dry with materialThe chloroform layer was dried
  10. filtrationfiltered
  11. customThe filtrate was evaporated under reduced pressure

Sources & evidence

ORD record
ord-0331d829dd6046beb94911093f01d680
Source dataset
uspto-grants-1983_09
Patent number
US04402973

Reaction notes

Loading…