HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-butyl 2-(6-methoxy-5-methyl-3-nitropyridin-2-yl)acetate → 2-(6-Methoxy-5-methyl-3-nitropyridin-2-yl)acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-butyl 2-(6-methoxy-5-methyl-3-nitropyridin-2-yl)acetate | HCID 44596705 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2-(6-Methoxy-5-methyl-3-nitropyridin-2-yl)acetic acid | HCID 44596706 | 94.4% |
Reaction Steps
A solution of tert-butyl 2-(6-methoxy-5-methyl-3-nitropyridin-2-yl)acetate (83.0 g, 294 mmol) from Part A in TFA (200 mL) was heated in a hot water bath for 1 h. The solution was concentrated in vacuo to give a brown oil. The oil was diluted with hexane and stirred. The resulting solid was collected by filtration and air dried to give 2-(6-methoxy-5-methyl-3-nitropyridin-2-yl)acetic acid (62.8 g, 94% yield) as a tan solid: 1H NMR (400 MHz, CDCl3) δ 8.70 (s br, 1H), 8.20 (s, 1H), 4.25 (s, 2H), 4.03 (s, 3H), 2.24 (s, 3H); 13C NMR (100 MHz, CDCl3) δ 175.59, 163.80, 146.52, 139.16, 135.30, 121.53, 54.86, 42.88, 15.32. An analytical sample was recrystallized from hexane: mp 135-137° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08436000B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-d8b0615091a1494ca54c7d0b51065cd0 |
| Source note | uspto-grants-2013_05 |