HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2060368Generated: November 1, 2026
Potassium Acetate → 1-Chloroisoquinolin-7-ol
https://huagongshe.com/reaction/2060368
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | Bis(pinacolato)diborane | HCID 2733548 | — |
| Reactant | 7-Bromo-1-Chloroisoquinoline | HCID 6502024 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Solvent | Sodium Bisulfate | HCID 516919 | — |
| Product | 1-Chloroisoquinolin-7-ol | HCID 46835415 | 94.5% |
Reaction Steps
7-Bromo-1-chloroisoquinoline (2.0 g, 8.25 mmol), bis(pinacolato)diboron (2.20 g, 8.66 mmol), potassium acetate (2.43 g, 24.7 mmol) and PdCl2(dppf)DCM adduct (0.337 g, 0.412 mmol) were combined under nitrogen in dioxane (40 mL) and heated in an oil bath at 100° C. for 24 h. The reaction mixture was cooled, diluted with EtOAc (100 mL) and washed with 10% aqueous KHSO4. The organic phase was dried over Na2SO4, filtered and concentrated to an oil. The oil was dissolved in acetone (100 mL) and a solution of OXONE (5.07 g, 8.25 mmol) in water (20 mL) added over 2 min. The reaction mixture was stirred for 10 min, diluted with aqueous sodium bisulfate solution and stirred for an additional 20 min. and then concentrated to remove acetone. The resulting mixture was filtered to give the title compound (1.4 g) which was used without further purification. LRMS (M+H)+=180.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08278322B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-dcb0f4f451be40969f610fb1e7728413 |
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| Source note | uspto-grants-2012_10 |
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