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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249373Generated: October 25, 2026

Bromomethyl methyl ether → 1-Bromo-4-chloro-2-fluoro-3-(methoxymethyl)benzene

https://huagongshe.com/reaction/2249373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromomethyl methyl etherHCID 83093—
Reactant1-Bromo-4-chloro-2-fluorobenzeneHCID 137275—
ReactantLithium diisopropylamideHCID 2724682—
SolventTetrahydrofuranHCID 8028—
Product1-Bromo-4-chloro-2-fluoro-3-(methoxymethyl)benzeneHCID 6880938171%

Reaction Conditions

Temperature-20 °C

Reaction Steps

A solution of 1-bromo-4-chloro-2-fluorobenzene (20.4 g, 0.100 mol) in THF (50 mL) was slowly added to LDA (0.125 mol) in THF (600 mL) at −50° C. After addition the solution was warmed to −20° C. and then cooled to −50° C. a solution of bromomethoxymethane (25 g, 0.200 mol) in THF (25 mL) was slowly added and the reaction mixture was warmed to ambient temperature. The reaction was quenched with water (400 mL) and extracted with diethyl ether (2×150 mL). The combined organic phases were dried (sodium sulfate) and concentrated. The residual oil was distilled (70°-75° C./0.5 mm) to give 1-bromo-4-chloro-2-fluoro-3-methoxymethylbenzene (18.0 g, 0.071 mol): 1H NMR (CDCl3): δ 7.50 (m, 1H), 7.15 (dd, 1H), 4.65 (s, 1H), 3.40 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07314849B2
Source datasetuspto-grants-2008_01
ORD IDord-ac2da014daba480d85a8943209a2482b
Source noteuspto-grants-2008_01