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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257526Generated: November 1, 2026

Pyridine → tert-butyl 3-bromo-5-[(E)-hydroxyiminomethyl]benzoate

https://huagongshe.com/reaction/1257526

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantTert-butyl 3-bromo-5-formylbenzoateHCID 58095966—
Solvent1,4-DioxaneHCID 31275—
Producttert-butyl 3-bromo-5-[(E)-hydroxyiminomethyl]benzoateHCID 58096166—

Reaction Conditions

Temperature68 °C

Reaction Steps

To a solution of tert-butyl 3-bromo-5-formylbenzoate (119 g, 417 mmol) in dioxane (2.4 L) were added hydroxylamine hydrochloride (44.0 g, 633 mmol) and pyridine (103 mL, 1.27 mol). The reaction mixture was heated to 68° C. After 16 h, the mixture was concentrated. Saturated aqueous amonium chloride was added the mixture was extracted with dichloromethane (3×). The combined organic extracts were washed with brine, dried over magnesium sulfate, filtered and concentrated (125.0 g). MS 243 (M-tert-butyl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461185B2
Source datasetuspto-grants-2013_06
ORD IDord-cf7ad118e908404e8bac483fe30a10c1
Source noteuspto-grants-2013_06