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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178244Generated: October 30, 2026

Sodium hydride → HCID 59418768, compound

https://huagongshe.com/reaction/2178244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantBenzene, (3-bromopropoxy)-HCID 68522—
ReactantMethyl 6-bromo-3-hydroxypicolinateHCID 22175135—
SolventCitric AcidHCID 311—
SolventDimethylacetamideHCID 31374—
ProductHCID 59418768HCID 5941876886%

Reaction Conditions

Temperature100 °C

Reaction Steps

Sodium hydride (60% in mineral oil, 172 mg, 4.53 mmol) was added to a mixture of methyl 6-bromo-3-hydroxypicolinate (26B) (1.0 g, 4.31 mmol) and 3-phenoxypropyl bromide (927 mg, 4.31 mmol) in DMA (20 mL) at it. The mixture was heated to 100° C. for 1.75 hours, cooled, diluted with 10% citric acid and extracted with EtOAc. The organic phases were washed with brine, dried over Na2SO4, and concentrated under reduced pressure. The crude material was purified by flash column chromatography on silica gel eluting with a gradient of PE:EtOAc 100:0-75:25, to provide 1.35 g (86%) of the desired product methyl 6-bromo-3-(3-phenoxypropoxy)picolinate (26C): 1H NMR (300 MHz, CDCl3) δ 7.52 (1H, d), 7.27 (2H, m), 6.92 (2H, m), 4.25 (2H, t), 4.19 (2H, t), 3.92 (3H, s), 2.30 (2H, t).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067928B2
Source datasetuspto-grants-2015_06
ORD IDord-674c4ba048a34b9b8642a8b3ce4ecb2c
Source noteuspto-grants-2015_06