Sodium Hydroxide → 5,7-Dichloro-2,3-dihydro-4-hydrazino-2-methylbenzofuran

HRID 1638930Notes

Reaction equation

HRID 1638930 reaction equation
[NH2:1][C:2]1[C:7]2[CH2:8][CH:9]([CH3:11])[O:10][C:6]=2[C:5]([Cl:12])=[CH:4][C:3]=1[Cl:13].[N:14]([O-])=O.[Na+].[Sn](Cl)Cl.[OH-].[Na+]>OS(O)(=O)=O.O.Cl>[Cl:13][C:3]1[CH:4]=[C:5]([Cl:12])[C:6]2[O:10][CH:9]([CH3:11])[CH2:8][C:7]=2[C:2]=1[NH:1][NH2:14]

Participants

8

Conditions

Temperature
0 °C

Procedure

2.19 g of 38A was suspended in 9 mL of concentrated H2SO4 and 9 mL of water at -5° C. A solution of 0.69 g of sodium nitrite in 4 mL of H2O was added slowly and the resulting solution was stirred at 0° C. for one hour. This solution was added slowly to a mixture of 4.51 g of tin (II) chloride in 15 mL of concentrated hydrochloric acid which was precooled to -10° C., so as to maintain -10° C. to -5° C. The mixture was slowly warmed to room temperature and stirred for 16 hours. With cooling, 50% sodium hydroxide solution was added to adjust the pH to 11. The mixture was extracted with ether. The extract was washed with water, brine, dried (MgSO4) and stripped of solvent to leave crude 5,7-dichloro-2,3-dihydro-4-hydrazino-2-methylbenzofuran (38B), as pale orange solid, m.p.: 59°-64° C.

Workup

  1. customat -5° C
  2. customwas precooled to -10° C.
  3. temperatureso as to maintain -10° C. to -5° C
  4. temperatureThe mixture was slowly warmed to room temperature
  5. stirringstirred for 16 hours
  6. temperatureWith cooling
  7. extractionThe mixture was extracted with ether
  8. washThe extract was washed with water, brine
  9. dry with materialdried (MgSO4)

Sources & evidence

ORD record
ord-4941107002724fd0bc3e18701ec1c142
Source dataset
uspto-grants-1989_11
Patent number
US04881967

Reaction notes

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