HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492105Generated: October 25, 2026
Phosphorus oxychloride → 1-Chlorophthalazine hydrochloride
https://huagongshe.com/reaction/492105
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 178518889 | HCID 178518889 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-Chlorophthalazine hydrochloride | HCID 22386464 | — |
Reaction Steps
A 3-neck 2 L round-bottomed flask was charged with phosphorous oxychloride (306 g, 2 mol. eq.) and cooled to about 0 to 5° C. To this was added 73 g of powdered phthalazinone (0.5 mol eq.). The reaction mass appeared as a suspension and was heated to about 60° C. with stirring. The progress of the reaction was monitored by HPLC. While the reaction mixture was maintained at approximately 50° C., about 65% of the phosphorous oxychloride was distilled out under vacuum. The concentrated reaction mixture was cooled to room temperature, about 375 mL of ethyl acetate was added, and then the mixture was purged with HCl gas for about 30 min.; thereafter, the mixture was cooled to a temperature of 0 to 5° C. and stirred for about one hour. The resulting pale yellow material was filtered and washed with 150 mL of cold ethyl acetate. The isolated material was 1-chlorophthalazine hydrochloride, which was dried under vacuum for about 3 hrs at 30° C. Yield =65%; purity=99%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07531653B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-548bcdd2f20f48c4bbe635dd4e5100c8 |
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| Source note | uspto-grants-2009_05 |
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