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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592397Generated: October 31, 2026

Acetic Anhydride → Acetic acid 1-methyl-1-(2-methyl-pyridin-3-yl)-ethyl ester

https://huagongshe.com/reaction/1592397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant2-(2-Methylpyridin-3-yl)propan-2-olHCID 45091732—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductAcetic acid 1-methyl-1-(2-methyl-pyridin-3-yl)-ethyl esterHCID 6727208075%

Reaction Conditions

Temperature100 °C

Reaction Steps

2-(2-methyl-pyridin-3-yl)-propan-2-ol (1.30 g, 8.61 mmol) and DMAP (30 mg) were combined in Ac2O (8 mL) and stirred at 100° C. for 16 hours. Following removal of the solvent under reduced pressure, the brown residue was quenched with saturated NaHCO3 (50 mL) and extracted with CH2Cl2 (5×60 mL). The combined organic extracts were dried (Na2SO4), filtered, and concentrated in vacuo to afford a yellow oil. Purification via column chromatography on silica gel (CH2Cl2:MeOH, 95:5, v/v) afforded acetic acid 1-methyl-1-(2-methyl-pyridin-3-yl)-ethyl ester as a white crystalline solid (1.25 g, 75%). 1H NMR (CDCl3) δ 1.80 (s, 3H), 2.05 (s, 3H), 2.66 (s, 3H), 7.12 (dd, 1H, J=9.0, 6.0 Hz), 7.62 (dd, 1H, J=9.0, 3.0 Hz), 8.39 (dd, 1H, J=6.0, 3.0 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291631B2
Source datasetuspto-grants-2007_11
ORD IDord-d00dd014feb44710b58516897a39f1b9
Source noteuspto-grants-2007_11