HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35626Generated: October 29, 2026
Phosphorus oxychloride → N-[3-(6-Chloro-3-pyridazinyl)phenyl]acetamide
https://huagongshe.com/reaction/35626
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | N-[3-(1,6-Dihydro-6-oxo-3-pyridazinyl)phenyl]acetamide | HCID 15595699 | — |
| Product | N-[3-(6-Chloro-3-pyridazinyl)phenyl]acetamide | HCID 15595701 | — |
Reaction Steps
A solution of 4.0 g of N-[3-(1,6-dihydro-6-oxo-3-pyridazinyl)phenyl]acetamide in 100 ml of phosphorus oxychloride was heated at 55°-65° C. for 1.5 hours and then the excess phosphorus oxychloride was removed in vacuo. The residue was dissolved in dichloromethane and the solution poured onto 200 g of crushed ice. After stirring for 30 minutes the acidic mixture was neutralized with aqueous sodium bicarbonate. The mixture was filtered, giving 0.8 g of solid. The dichloromethane layer of the filtrate was separated, dried and evaporated, giving 2.93 g of solid. The two solids were combined (3.73 g) and a 2.9 g portion chromatographed on a silica gel column, eluting with dichloromethane-methanol (95:5). The fractions containing product were combined, evaporated and the solid (1.5 g) recrystallized from dichloromethane-acetone, to give the desired compound as tan crystals, mp 203°-205° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04767765 |
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| Source dataset | uspto-grants-1988_08 |
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| ORD ID | ord-5fc55e4b86284ac4ade352367407fa84 |
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| Source note | uspto-grants-1988_08 |
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