HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207566Generated: October 23, 2026
2,2-Difluoro-2-(fluorosulfonyl)acetic acid → Ethyl 6-difluoromethoxymethylpyridine-2-carboxylate
https://huagongshe.com/en/reaction/2207566
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,2-Difluoro-2-(fluorosulfonyl)acetic acid | HCID 2737516 | — |
| Reactant | 2-Pyridinecarboxylic acid, 6-(hydroxymethyl)-, ethyl ester | HCID 10921141 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl 6-difluoromethoxymethylpyridine-2-carboxylate | HCID 66718372 | 13% |
Reaction Steps
2,2-Difluoro-2-(fluorosulfonyl)acetic acid (495 mL, 4.79 mmol) was added dropwise to a solution of ethyl 6-hydroxymethylpyridine-2-carboxylate (800 mg, 4.79 mmol) and CuI (91 mg, 0.479 mmol) in MeCN (10 mL) at room temperature at a rate to maintain the internal temperature <30° C. The mixture was stirred for a further 20 min at room temperature, poured onto brine/water and extracted with EtOAc (×3). The combined extracts were dried (MgSO4), filtered, evaporated and purified by column chromatography (4:1 to 2:1, isohexane:EtOAc) to give the title compound (130 mg, 13%) as a colorless oil; NMR δH (400 MHz, CDCl3) 8.01 (1H, d, J 7.5 Hz), 7.89 (1H, t, J 7.5 Hz), 7.66 (1H, d, J 7.5 Hz), 6.41 (1H, t, J 74.0 Hz), 5.14 (2H, s), 4.49 (2H, q, J 7.0 Hz), 1.44 (3H, t, J 7.0H); (M+H)+ 232.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09376443B2 |
|---|
| Source dataset | uspto-grants-2016_06 |
|---|
| ORD ID | ord-2d1c22284e88425181549ff89db4af20 |
|---|
| Source note | uspto-grants-2016_06 |
|---|