HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422541Generated: October 30, 2026
Phosphorus oxychloride → 6-Bromo-1-chlorophthalazine
https://huagongshe.com/reaction/422541
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 178518884 | HCID 178518884 | — |
| Product | 6-Bromo-1-chlorophthalazine | HCID 22030424 | 67.1% |
Reaction Steps
A mixture of 6-bromophthalazin-1(2H)-one (17, 2.6 g, 12 mmol) in phosphorous oxychloride (11 mL, 116 mmol) was treated with diisopropylethylamine (2.0 mL, 12 mmol). The mixture was stirred at room temperature for 30 min, then warmed up to a temperature of between about 95-100° C. and stirred under nitrogen. The suspension (reaction) became a deep brown solution in about 30 min, then a yellow solid precipitated out. After about 3 h, all of the starting material was converted, as appeared by TLC, to product (M+1=243, 245). After the mixture was cooled down to room temperature, it was diluted with 50 mL CHCl3 and cooled down to 0° C. The precipitate was filtrated, washed with 10 mL ice cool CHCl3, collected and dried under vacuum, to afford 1.96 g of 6-bromo-1-chlorophthalazine 18, as yellow solid. Found MS (ES+): 243, 245 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08101612B2 |
|---|
| Source dataset | uspto-grants-2012_01 |
|---|
| ORD ID | ord-65fd772f22014a3eae91d30e0fecedd6 |
|---|
| Source note | uspto-grants-2012_01 |
|---|