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

HRID 1709127Notes

Reaction equation

HRID 1709127 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-8e89f35bc8874fb49d19d6a0154071de
Source dataset
uspto-grants-1990_08
Patent number
US04948418

Reaction notes

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