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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 859081Generated: October 25, 2026

Dimethylformamide → 1,1'-Biphenyl, 2,2'-bis(methoxymethoxy)-

https://huagongshe.com/reaction/859081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantTetrahydrofuranHCID 8028—
Reactant(1,1'-Biphenyl)-2,2'-diolHCID 15731—
ReactantSodium hydrideHCID 24758—
Product1,1'-Biphenyl, 2,2'-bis(methoxymethoxy)-HCID 1147132197%

Reaction Steps

To a 250 mL of three-necked bottle was added NaH (content 50%, 3.5 g, 72 mmol), anhydrous THF (60 mL) and anhydrous DMF (20 mL), after the temperature was lowered to 0° C., a solution of biphenol (5.6 g, 30 mmol) in THF (15 mL) was added, stirred at this temperature for 10 minutes. Methoxymethyl chloride (6 mL, 78 mmol) was added dropwise, and the mixture was stirred for 8 h at room temperature, quenched by adding 100 mL of water, extracted with ethyl acetate (100 mL×3), the combined organic phase was washed with brine (60 mL×2), dried over MgSO4, after filtration, the solvent was removed to give a yellow oil. Purification through chromatography give 8 g (97% yield) of the product as a light yellow oil. 1HNMR (300 MHz, CDCl3) δ (ppm) 3.39 (s, 6H), 5.12 (s, 4H), 7.13 (m, 2H), 7.30–7.37 (m, 6H). Physical data of the compound was consistent with that reported in literature.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07151070B2
Source datasetuspto-grants-2006_12
ORD IDord-d4e93b93b1a240b8be74ac423b42f8aa
Source noteuspto-grants-2006_12