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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 78263Generated: October 26, 2026

Chloromethyl Methyl Ether → 1-Bromo-3-[(methoxymethoxy)methyl]benzene

https://huagongshe.com/reaction/78263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantSodium hydrideHCID 24758—
Reactant3-Bromobenzyl alcoholHCID 85141—
SolventTetrahydrofuranHCID 8028—
Product1-Bromo-3-[(methoxymethoxy)methyl]benzeneHCID 1144757883%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a tetrahydrofuran (100 mL) solution of 3-bromobenzyl alcohol (10 g, 54 mmol) was added sodium hydride (2.3 g, 98 mmol, 60% in oil) at room temperature. Then, chloromethyl methyl ether (5.2 g, 64 mmol) was added to this suspension, which was stirred for 15 minutes at 60° C. This mixture was partitioned into ethyl acetate and water. The organic layer was separated and concentrated under a reduced pressure. The residue was purified by silica gel column chromatography (heptane:ethyl acetate=8:1) to obtain the title compound (10 g, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841327B2
Source datasetuspto-grants-2014_09
ORD IDord-4203a6b99c9c41c7b61a2107c2ecb1da
Source noteuspto-grants-2014_09