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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2197542Generated: November 2, 2026

Sodium Hydroxide → 5-Bromo-6-methoxypyridine-3-carbaldehyde

https://huagongshe.com/reaction/2197542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantBromineHCID 24408—
ReactantSodium AcetateHCID 517045—
Reactant6-Methoxypyridine-3-carbaldehydeHCID 3364576—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product5-Bromo-6-methoxypyridine-3-carbaldehydeHCID 1239241639.2%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a mixture of 6-methoxynicotinaldehyde (3 g, 0.0219 mol) and NaOAc (3.5 g, 0.0427 mol) in HOAc (10 mL) was added a solution of bromine (1.64 mL, 0.031 mol) in HOAc (10 mL) over 30 mins via an additional funnel. The mixture was heated to 90° C. for 5 h, cooled to rt. The reaction was added iced water (100 mL), neutralized to pH=7.5 with aq. NaOH (5 N), extracted with ethyl acetate (4×50 mL), washed with brine, dried over Na2SO4, filtered and concentrated. The residue was purified via flash column using dichloromethane as an eluent. The product containing fractions were collected and concentrated to give 5-bromo-6-methoxynicotinaldehyde (1.854 g, 39% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338604B2
Source datasetuspto-grants-2012_12
ORD IDord-942d22f1c19043a69e8afbb0089bc130
Source noteuspto-grants-2012_12