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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 632426Generated: October 27, 2026

Methanol → Methyl 5-bromo-6-(isobutylthio)picolinate

https://huagongshe.com/reaction/632426

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSulfuric AcidHCID 1118—
Reactant5-Bromo-6-(isobutylthio)picolinic acidHCID 71087437—
SolventSodium chloride; waterHCID 57417360—
ProductMethyl 5-bromo-6-(isobutylthio)picolinateHCID 7108720539%

Reaction Conditions

Temperature80 °C

Reaction Steps

5-Bromo-6-(isobutylthio)picolinic acid (500 mg, 1.72 mmol) was dissolved in methanol (5 mL) to give a yellow solution. Sulfuric acid (169 mg, 92.3 μL, 1.72 mmol) was added. The reaction mixture was heated to 80° C. and stirred for 1 d. The reaction mixture was cooled to 0° C. and poured onto icewater/brine (25 mL). The aqueous layer was extracted with EtOAc (2×40 mL) and washed with icewater/brine (20 mL). The organic layers were combined, dried over Na2SO4 and concentrated in vacuo to give crude title compound as a yellow oil. The oil was purified by flash chromatography (silica gel, 5 g, 0% to 15% EtOAc in heptane) to give the title product (205 mg, 39%) as a colorless oil. MS (EI): m/e=306.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321727B2
Source datasetuspto-grants-2016_04
ORD IDord-ed25b38f0b3f4d44b6c5d563c86430e9
Source noteuspto-grants-2016_04