HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118211Generated: October 26, 2026
Water → 1-[4-(Methoxymethoxy)phenyl]-2-phenylbutan-1-one
https://huagongshe.com/reaction/2118211
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | 1-Bromo-4-(methoxymethoxy)benzene | HCID 10465919 | — |
| Reactant | N-methoxy-N-methyl-2-phenylbutanamide | HCID 11229537 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-[4-(Methoxymethoxy)phenyl]-2-phenylbutan-1-one | HCID 58877661 | 80% |
Reaction Steps
To a stirred solution of 13 (99.0 g, 0.46 mol) in anhydrous THF (750 mL) was added n-BuLi (1.6 M in hexanes, 310 mL, 0.50 mol) dropwise at −78° C. The reaction mixture was stirred for 30 min and 14 (90.1 g, 0.43 mol) dissolved in THF (500 mL) was added dropwise. The reaction mixture was stirred at −78° C. for 1 h and then slowly warmed to 0° C. H2O (500 mL) was added and the volatiles were removed under reduced pressure. The residue was extracted with Et2O (3×500 mL) and the combined extracts were washed with water (500 mL) and brine (500 mL). The mixture was dried over MgSO4 and concentrated. The residue was recrystallized from hexanes to afford 97.6 g (80%) of 15 as white needles. 1HNMR (400 MHz, DMSO-d6): δ 0.79 (t, J=7.3 Hz, 3H), 1.68 (h, J=7.0 Hz, 1H), 2.03 (h, J=7.0 Hz, 1H), 3.32 (s, 3H), 4.65 (t, J=7.3 Hz, 1H), 5.21 (s, 2H), 7.03 (d, J=8.8 Hz, 2H), 7.15 (t, J=7.1 Hz, 1H), 7.23-7.30 (m, 4H), 7.98 (d, J=8.8 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-ca876288d4d643b6b27e67bd9dea86a2 |
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| Source note | uspto-grants-2008_10 |
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