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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Chloromethyl Methyl Ether | HCID 7864 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | (1,1'-Biphenyl)-2,2'-diol | HCID 15731 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Product | 1,1'-Biphenyl, 2,2'-bis(methoxymethoxy)- | HCID 11471321 | 97% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07151070B2 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-d4e93b93b1a240b8be74ac423b42f8aa |
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| Source note | uspto-grants-2006_12 |
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