HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → Methyl 3-fluoro-2-formylpyridine-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Ozone | HCID 24823 | — |
| Reactant | 3-Fluoro-2-vinyl-isonicotinic acid methyl ester | HCID 69672774 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 3-fluoro-2-formylpyridine-4-carboxylate | HCID 86666496 | — |
Reaction Steps
Ozone was bubbled through a solution of methyl 3-fluoro-2-vinylisonicotinate (1.4 g, 7.73 mmol, from Step 2) in methylene chloride (100 mL) at −78° C. until the blue color of excess ozone persisted. Nitrogen was bubbled through the solution for 1 minute to purge excess ozone and then triphenylphosphine (3.9 g, 15 mmol) was added and the solution was warmed to room temperature and stirred overnight. The compound was dry loaded onto silica gel. Flash chromatography eluting with 40% ethyl acetate in hexanes afforded product (0.8 g, 57%) as an off-white crystalline solid. 1H NMR (300 MHz, CDCl3): δ 10.27 (s, 1H), 8.73 (d, 1H), 8.01 (dd, 1H), 4.01 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08933085B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-d70aede932974ef28b9e4567297aed72 |
| Source note | uspto-grants-2015_01 |