HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344607Generated: October 29, 2026
Sodium Hydroxide → 5,7-Dichloro-2,3-dihydro-4-hydrazino-2-methylbenzofuran
https://huagongshe.com/reaction/344607
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Stannous Chloride | HCID 24479 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | 4-Amino-5,7-dichloro-2,3-dihydro-2-methylbenzofuran | HCID 53971178 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 5,7-Dichloro-2,3-dihydro-4-hydrazino-2-methylbenzofuran | HCID 54549881 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05053071 |
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| Source dataset | uspto-grants-1991_10 |
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| ORD ID | ord-746efa9c4e1b4104b59ce3850a21eb3c |
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| Source note | uspto-grants-1991_10 |
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