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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Peracetic Acid | HCID 6585 | — |
| Reactant | HCID 58042455 | HCID 58042455 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | 5-Chloro-6-isopropoxypyridin-3-OL | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09102621B2 |
|---|
| Source dataset | uspto-grants-2015_08 |
|---|
| ORD ID | ord-e8b91d5b28ca4a76a5edb855807babb2 |
|---|
| Source note | uspto-grants-2015_08 |
|---|