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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1461006Generated: October 25, 2026

Methanol → 11-Methoxyundecanoic acid

https://huagongshe.com/reaction/1461006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPotassium HydroxideHCID 14797—
Reactant11-Bromoundecanoic acidHCID 17812—
Product11-Methoxyundecanoic acidHCID 3804742.5%

Reaction Steps

11-bromoundecanoic acid (10.0 g, 37.7 mmol) was added to a solution of potassium hydroxide (24.3 g, 433 mmol) in methanol (280 mL) and refluxed for 5 hrs. After cooling and acidification with HCl, solvent was removed under reduced pressure. The sample was dissolved in ethyl acetate and extracted with water. The organic phase was dried over sodium sulfate, and the solvent removed under reduced pressure. The product was purified by silica column chromatography using increasing concentrations of ethyl acetate in hexanes for elution. The product eluted in 25% ethyl acetate in hexanes. Solvent was removed under reduced pressure to give 11-(methoxy)undecanoic acid (200 mg, 2.5%): mp 31-32° C.; 1H NMR (300 MHz, CDC13) δ 1.1-1.3 (bm, 12H, methylene envelope). 1.45-1.63 (bm. 4H, O-CH2 --CH2, CH2 --CH2 --COOH), 2.34 (t, 2H, J=7.3, CH2 --COOH), 3.45 (s, 3H, CH3), 3.50 (t, 2H, J=6.8, 0--CH2), 10.70 (br, COOH); 13C NMR (75.4 MHz, CDC13) δ 24.64, 26.00, 29.00, 29.16, 29.29, 29.40, 34.00, 58.23, 72.81, 179.17; m/z 216 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05073571
Source datasetuspto-grants-1991_12
ORD IDord-25f2a766420448c0b81b02c404f4f1c2
Source noteuspto-grants-1991_12