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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253253Generated: November 1, 2026

Tetrahydrofuran → (2-(Methyloxy)-3-{[2-(methyloxy)ethyl]oxy}phenyl)methanol

https://huagongshe.com/reaction/253253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantMethyl 2-(methyloxy)-3-{[2-(methyloxy)ethyl]oxy}benzoateHCID 66890135—
Product(2-(Methyloxy)-3-{[2-(methyloxy)ethyl]oxy}phenyl)methanolHCID 6689142378%

Reaction Steps

To a solution of methyl 2-(methyloxy)-3-{[2-(methyloxy)ethyl]oxy}benzoate (0.54 g, 2.3 mmol) at 0° C. was added a solution of lithium aluminum hydride in tetrahydrofuran (1M, 2.8 mL, 2.8 mmol) and the resulting mixture was stirred for one hour. It was then quenched with ethyl acetate (1 mL) and 5% sodium hydroxide solution (1 mL), diluted with ether (100 mL), and filtered. The filtrate was washed water and brine (100 mL each), dried over sodium sulfate, filtered and concentrated to give (2-(methyloxy)-3-{[2-(methyloxy)ethyl]oxy}phenyl)methanol (0.37 g, 1.7 mmol, 78% yield). 1H NMR (400 MHz, CDCl3): 7.02-6.93 (d, d, 1H), 6.92-6.87 (m, 2H), 4.68 (s, 2H), 4.16-4.14 (m, 2H), 3.92 (s, 3H), 3.79-3.77 (m, 2H), 3.45 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872014B2
Source datasetuspto-grants-2011_01
ORD IDord-8792e02bf6d045d9a3a435e81559d405
Source noteuspto-grants-2011_01