Water → (2-Amino-3-chlorophenyl)methanol

HRID 844992Notes

Reaction equation

HRID 844992 reaction equation
[Cl:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:4]([C:5](OC)=[O:6])[C:3]=1[NH2:12].[H-].[Al+3].[Li+].[H-].[H-].[H-].O.[OH-].[Na+]>CCOCC>[NH2:12][C:3]1[C:2]([Cl:1])=[CH:11][CH:10]=[CH:9][C:4]=1[CH2:5][OH:6]

Participants

6

Procedure

A solution of 28.9 g (155 mmol) of methyl 3-chloro-anthranilate in 100 ml of ether was added dropwise to a stirred suspension of 7.67 g (202 mmol) of lithium aluminum hydride in 400 ml of ether. After stirring for 5 hours at room temperature, the grey mixture was treated sequentially with 7.7 ml of water, 7.7 ml of 15% sodium hydroxide and 23 ml of water. The reaction mixture was filtered, and the filtrate was evaporated at reduced pressure. The oily residue was dissolved in ether, and precipitation of the product was induced by addition of hexane. The product was collected by filtration to yield a tan solid in 67% yield, m.p. 56°-68° C. IR and 1H NMR spectra were in agreement with the assigned structure.

Workup

  1. filtrationThe reaction mixture was filtered
  2. customthe filtrate was evaporated at reduced pressure
  3. dissolutionThe oily residue was dissolved in ether
  4. customprecipitation of the product
  5. additionwas induced by addition of hexane
  6. filtrationThe product was collected by filtration
  7. customto yield a tan solid in 67% yield, m.p. 56°-68° C

Sources & evidence

ORD record
ord-592b0e68a9ef40f184dfc3c28f5642ed
Source dataset
uspto-grants-1988_07
Patent number
US04755212

Reaction notes

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