HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2048046Generated: November 1, 2026
Peracetic Acid → 5-Chloro-6-isobutoxypyridin-3-OL
https://huagongshe.com/reaction/2048046
Participants
| Role | Name | HCID | Charge |
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| Reactant | Peracetic Acid | HCID 6585 | — |
| Reactant | 3-Chloro-2-isobutoxypyridine-5-boronic acid | HCID 46739600 | — |
| Solvent | Acetic acid--water (1/1) | HCID 21899381 | — |
| Product | 5-Chloro-6-isobutoxypyridin-3-OL | HCID 58042500 | 138.6% |
Reaction Steps
To a suspension of 5-chloro-6-isobutoxypyridin-3-ylboronic acid (3.02 g, 13.1 mmol) in acetic acid/water (1:1, 20 mL) cooled to 0° C. was slowly added peracetic acid (3.9 mL, 20.0 mmol) and the reaction mixture was maintained at 0° C. for 1.5 hours and then at room temperature for 1 hour. Additional peracetic acid (3.9 mL, 20.0 mmol) was added and the reaction stirred at room temperature for 40 minutes after which time the suspension dissolved. The reaction mixture was quenched with sodium thiosulphate solution (15 mL) and stirred for 5 minutes. The mixture was extracted with EtOAc (2×30 mL) and the combined organic extracts washed with brine (30 mL), dried over magnesium sulfate and filtered. The solvent was removed under reduced pressure to afford a yellow oil (3.66 g). The oil was purified by silica gel chromatography (Biotage™ 50 g) eluting with 80 to 100% methanol in DCM to afford the title compound as a white solid (1.94 g, 73%):
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08592629B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-a1d289454fd94a05873af92f6b525909 |
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| Source note | uspto-grants-2013_11 |
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