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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457535Generated: October 30, 2026

Sodium Bicarbonate → 1-Bromo-3-methoxymethoxy-5-vinyl-benzene

https://huagongshe.com/reaction/457535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant3-Bromo-5-methoxymethoxy-benzaldehydeHCID 19261595—
ReactantButyllithiumHCID 178418339—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product1-Bromo-3-methoxymethoxy-5-vinyl-benzeneHCID 1843996376%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of n-BuLi (5.65 mL of a 1.6 M solution in Et2O, 9.04 mmol) was added dropwise to a solution of methyltriphenylphosphonium bromide (3.23 g, 9.05 mmol) in THF (15 mL) that was cooled to 0° C. The resulting yellow solution was stirred for 30 m, cooled to −78° C., and a solution of 3-bromo-5-methoxymethoxy-benzaldehyde (1.58 g, 6.46 mmol) in anhydrous THF (15 mL) was added dropwise. The mixture was slowly warmed to RT, stirred for 16 h, and then added to a saturated aqueous solution of NaHCO3 (60 mL). The layers were separated, and the aqueous layer was extracted with Et2O (2×50 mL). The combined organic layers were washed with brine (30 mL), and dried with anhydrous MgSO4. The volatile materials were evaporated, and the remaining oil was purified by flash chromatography on silica gel (0% to 3% EtOAc/hexanes) to provide 600 mg (76%) of 1-bromo-3-methoxymethoxy-5-vinyl-benzene (113c).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07189718B2
Source datasetuspto-grants-2007_03
ORD IDord-a95c43220bdd42249fec4cf5ecd5eace
Source noteuspto-grants-2007_03