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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088514Generated: November 3, 2026

Tert-butyl 2-(6-methoxy-5-methyl-3-nitropyridin-2-yl)acetate → 2-(6-Methoxy-5-methyl-3-nitropyridin-2-yl)acetic acid

https://huagongshe.com/reaction/2088514

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 2-(6-methoxy-5-methyl-3-nitropyridin-2-yl)acetateHCID 44596705—
SolventTrifluoroacetic acidHCID 6422—
SolventHexaneHCID 8058—
Product2-(6-Methoxy-5-methyl-3-nitropyridin-2-yl)acetic acidHCID 4459670694.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436000B2
Source datasetuspto-grants-2013_05
ORD IDord-d8b0615091a1494ca54c7d0b51065cd0
Source noteuspto-grants-2013_05