HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359148Generated: October 26, 2026
Chloromethyl Methyl Ether → 2,5-Diphenyl-3-(methoxymethoxy)-thiophene
https://huagongshe.com/reaction/359148
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloromethyl Methyl Ether | HCID 7864 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,5-Diphenylthiophene-3-ol | HCID 15078738 | — |
| Reactant | Diethylether water | HCID 21584184 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2,5-Diphenyl-3-(methoxymethoxy)-thiophene | HCID 15078740 | 87.7% |
Reaction Steps
To a stirred, ice cooled solution of 2,5-diphenyl-3-hydroxythiophene (0.12 g, 0.5 mmol) in dried N,N-dimethylformamide (2 ml) was added sodium hydride (30 mg of a 60% suspension in mineral oil). When the initial vigorous reaction subsides (ca. 4 minutes), the mixture was allowed to stir at ambient temperatures for 20 minutes and then recooled. Chloromethyl methyl ether (0.055 ml, 0.7 mmol) was then added all at once. After stirring cold for ca. 30 minutes, the mixture was allowed to stir at ambient temperatures for ca. 4 hours and then added to a stirred ether/water mixture. The ether layer was washed 3 times with water, dried over sodium sulfate, filtered, concentrated to a residue, and chromatographed on silica gel (methylene chloride/hexane), to yield 0.13 g of (II). M.S.: M+ =296; NMR: consistent. ##STR27##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04999436 |
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| Source dataset | uspto-grants-1991_03 |
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| ORD ID | ord-8ebe84a4a2734710adc20aa22273e31b |
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| Source note | uspto-grants-1991_03 |
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