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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 5-Bromo-6-(isobutylthio)picolinic acid | HCID 71087437 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | Methyl 5-bromo-6-(isobutylthio)picolinate | HCID 71087205 | 39% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09321727B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-ed25b38f0b3f4d44b6c5d563c86430e9 |
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| Source note | uspto-grants-2016_04 |
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