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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494659Generated: October 27, 2026

Pyridine → [2-Methoxy-1-(3-methylbutyl)-1,4-dihydronaphthalen-1-yl]methyl acetate

https://huagongshe.com/reaction/494659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
Reactant[2-Methoxy-1-(3-methylbutyl)-1,4-dihydronaphthalen-1-yl]methanolHCID 68871071—
SolventWaterHCID 962—
Product[2-Methoxy-1-(3-methylbutyl)-1,4-dihydronaphthalen-1-yl]methyl acetateHCID 6887246281%

Reaction Steps

A mixture of Example 179A (0.18 g, 0.7 mmol), acetic anhydride (0.2 mL), and pyridin (1 mL) was stirred at room temperature for 18 h. The solution was diluted with water (3 mL) and extracted with ethyl acetate (2× 1 mL). The combined organic extracts were dried (Na2SO4) and concentrated in vacuo. Column chromatography on silica (hexane to 5% ethyl acetate/hexane) afforded product as a colorless oil (0.17 g, 81%). 1H NMR (300 MHz, CDCl3) δ ppm 0.66 (m, 1H), 0.76 (dd, J=9.56, 6.62 Hz, 6H), 0.89 (m, 1H), 1.38 (m, 1H), 1.61 (m, 1H), 1.81 (s, 3H), 1.95 (m, 1H), 3.50 (s, 2H), 3.58 (s, 3H), 4.24 (d, J=10.66 Hz, 1H), 4.42 (d, J=10.66 Hz, 1H), 5.01 (t, J=3.49 Hz, 1H), 7.20 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538105B2
Source datasetuspto-grants-2009_05
ORD IDord-37d9b5aab7394de896e5a43d1f195122
Source noteuspto-grants-2009_05