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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118209Generated: October 31, 2026

Water → 1-Bromo-4-(methoxymethoxy)benzene

https://huagongshe.com/reaction/2118209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-BromophenolHCID 7808—
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantSodium hydrideHCID 24758—
SolventTetrahydrofuranHCID 8028—
Product1-Bromo-4-(methoxymethoxy)benzeneHCID 10465919918.2%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07442833B2
Source datasetuspto-grants-2008_10
ORD IDord-f97b05abb8034fc896f5f0008f923ca9
Source noteuspto-grants-2008_10