HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045035Generated: October 29, 2026
Potassium Phosphate, Tribasic → HCID 44540525, compound
https://huagongshe.com/reaction/1045035
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | 2-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl | HCID 11269872 | — |
| Reactant | HCID 44540523 | HCID 44540523 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 44540525 | HCID 44540525 | 24.4% |
Reaction Steps
170 mg of 7-bromo-1,1-dioxo-1H-1λ6-benzo[d]isothiazol-3-ylamine, 119 mg of phenylboronic acid, 10 mg of palladium(II)acetate, 21 mg of 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl and 415 mg of potassium phosphate are suspended in 5 ml of toluene. The mixture is stirred under an argon athmosphere at 100° C. for 16 h. The reaction mixture is poured into water and extracted with ethyl acetate. The organic phase is washed with water, dried over sodium sulfate and evaporated. Chromatographie of the residue with cyclohexane—ethyl acetate (1:1) affords 41 mg of 1,1-dioxo-7-phenyl-1H-1λ6-benzo[d]isothiazol-3-ylamine (P1.5).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08563744B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-20e8d571aa1d47ec85b46cfb2b6459df |
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| Source note | uspto-grants-2013_10 |
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