HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717540Generated: October 29, 2026
Dimethyl Sulfide → HCID 89463002, compound
https://huagongshe.com/reaction/717540
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | 3-Bromo-5-fluoropyridine | HCID 820206 | — |
| Reactant | HCID 178418630 | HCID 178418630 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 89463002 | HCID 89463002 | — |
Reaction Steps
Phenyl chloroformate (4.2 mL, 0.033 mol) was added to a mixture of 3-bromo-5-fluoro-pyridine (5.5 g, 0.031 mol), dimethyl sulphide (15.32 mL, 0.209 mol) and copper iodide (5.95 g, 0.031 mol) in anhydrous tetrahydrofuran (50 mL) at RT and the reaction mixture was stirred for 40-50 min. To this suspension, cyclopropylmagnesiumbromide (66.75 mL, 0.033 mol, 0.5 M solution in tetrahydrofuran) was added at −25 to −20° C. over a 30-40 min period. The mixture was stirred at this temperature for 30 min, and then warmed slowly to RT over 1.0-1.5 hrs. The reaction mixture was quenched with a saturated aqueous ammonium chloride solution (200 mL), followed by extraction of the aqueous layer with ethyl acetate (3×200 mL). The combined organic layers were washed with a saturated aqueous sodium chloride solution (2×100 mL), and dried over anhydrous sodium sulphate to afford the crude compound, which was purified by silica gel chromatography using 0-5% ethyl acetate-hexane gradient. This yielded crude phenyl 3-bromo-4-cyclopropyl-5-fluoro-4H-pyridine-1-carboxylic acid phenyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193724B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-cc5084c651f34f908a3e5e9ce1bb2f5e |
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| Source note | uspto-grants-2015_11 |
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