Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Bromophenol | HCID 7808 | — |
| Reactant | Chloromethyl Methyl Ether | HCID 7864 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Bromo-4-(methoxymethoxy)benzene | HCID 10465919 | 918.2% |
Reaction Steps
To a suspension of 60% NaH in mineral oil (12.7 g, 31.8 mmol) in anhydrous THF (300 mL) at 0° C. was added 4-bromophenol (50.0 g, 28.9 mmol) dissolved in THF (100 mL) dropwise over 1 h. The reaction mixture was stirred at 0° C. for 30 min, and chloromethylmethyl ether (24.8 mL, 32.6 mmol) dissolved in THF (30 mL) was added dropwise over 20 min. The reaction mixture was stirred overnight at RT. H2O (250 mL) was added, and the mixture was extracted with Et2O (2×250 mL). The combined ethereal extracts were washed with brine (500 mL), dried over MgSO4, and concentrated. The residue was distilled under vacuum to afford 57.6 g (92%) of 13 as a colorless oil. 1H NMR (400 MHz, DMSO-d6): δ 3.33 (s, 3H), 5.15 (s, 2H), 6.96 (d, J=9.0 Hz, 2H), 7.43 (d, J=9.0 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07442833B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-f97b05abb8034fc896f5f0008f923ca9 |
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| Source note | uspto-grants-2008_10 |
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