Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPeracetic AcidHCID 6585—
Reactant3-Chloro-2-isobutoxypyridine-5-boronic acidHCID 46739600—
SolventAcetic acid--water (1/1)HCID 21899381—
Product5-Chloro-6-isobutoxypyridin-3-OLHCID 58042500138.6%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592629B2
Source datasetuspto-grants-2013_11
ORD IDord-a1d289454fd94a05873af92f6b525909
Source noteuspto-grants-2013_11