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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 512036Generated: October 25, 2026

Water → 5-Chloro-6-isopropoxypyridin-3-OL

https://huagongshe.com/reaction/512036

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPeracetic AcidHCID 6585—
ReactantHCID 58042455HCID 58042455—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
SolventHeptaneHCID 8900—
Product5-Chloro-6-isopropoxypyridin-3-OLHCID 58042436—

Reaction Steps

To a solution of 3-chloro-2-isopropoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine (Preparation 7, 297.6 g, 897.9 mmol) in acetic acid:water (2.2 L:1.0 L) at 0° C. was added peracetic acid (191 mL, 1.077 mol) and the reaction was allowed to warm gradually to room temperature. After 4 hours the reaction was complete and was quenched with 0.5 M solution of sodium thiosulfate (225 mL). The resulting dark solution was evaporated to dryness and the residue was passed through a plug of silica (flushed with neat heptane follow by a gradient up to 10% ethyl acetate:heptane) to remove base line boronate salts. The filtrate was evaporated in vacuo to give a pale yellow viscous oil before further flash column chromatography was performed (1.5 kg for 80 g of material) using 30% ethylacetate in heptane as eluent) to provide a pale yellow solid which was triturated with heptane, dried under suction to give the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102621B2
Source datasetuspto-grants-2015_08
ORD IDord-e8b91d5b28ca4a76a5edb855807babb2
Source noteuspto-grants-2015_08