HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxyamine hydrochloride → 2-Chloro-6-fluoro-4-hydroxybenzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Formate | HCID 2723810 | — |
| Reactant | 2-Chloro-6-fluoro-4-hydroxybenzaldehyde | HCID 58402603 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | 2-Chloro-6-fluoro-4-hydroxybenzonitrile | HCID 117653144 | 56% |
Reaction Conditions
| Temperature | 105 °C |
|---|
Reaction Steps
A solution of 2-chloro-6-fluoro-4-hydroxybenzaldehyde (WO 2008141249, 90 mg, 0.344 mmol) in formic acid (1 mL) was treated with hydroxylamine hydrochloride (23.9 mg, 0.344 mmol) and sodium formate (23.4 mg, 0.344 mmol) and stirred under nitrogen for 3.5 hours at 105° C. The mixture was concentrated in vacuo and the residue treated with saturated aqueous sodium bicarbonate solution (10 mL). The aqueous solution was extracted with ethyl acetate (2×10 mL), dried over sodium sulphate and concentrated in vacuo. The residue was purified using silica gel column chromatography eluting with 30-50% EtOAc in heptanes to afford the title compound as a beige solid (33 mg, 56%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09067922B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-7c4afb027058457f87d1ff26f687dcdf |
| Source note | uspto-grants-2015_06 |