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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2100092Generated: November 1, 2026

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

https://huagongshe.com/reaction/2100092

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. Water (250 mL) was added, and the mixture was extracted with ether (3×250 mL). The combined ethereal extracts were washed with brine, dried (MgSO4), and concentrated. The residue was distilled under vacuum to afford 57.6 g (92%) of 86 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 numberUS07569601B2
Source datasetuspto-grants-2009_08
ORD IDord-9ae80471d7834eba82972a450bb6d16a
Source noteuspto-grants-2009_08