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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 216225Generated: October 30, 2026

Bis(2-bromoethyl) ether → Methyl 4-(3-bromophenyl)tetrahydro-2H-pyran-4-carboxylate

https://huagongshe.com/reaction/216225

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBis(2-bromoethyl) etherHCID 21521—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 2-(3-bromophenyl)acetateHCID 11746402—
SolventDimethylformamideHCID 6228—
ProductMethyl 4-(3-bromophenyl)tetrahydro-2H-pyran-4-carboxylateHCID 6709103877.8%

Reaction Steps

A solution of (3-bromo-phenyl)-acetic acid methyl ester (0.6 g, 2.62 mmol) in dry N,N′-dimethylformamide is added to a stirred suspension of sodium hydride (60% in mineral oil, 0.26 g, 6.55 mmol) in dry N,N′-dimethylformamide at 0° C. and stirring is continued for 20 minutes. A solution of bis(2-bromoethyl)ether (0.39 mL, 3.14 mmol) in N,N-dimethylformamide is added drop-wise and the reaction mixture is stirred overnight, while warming to room temperature. The reaction is quenched with water, extracted twice with ethyl acetate, the combined extracts is washed with brine and water, dried over sodium sulfate, filtered and concentrated in vacuo to afford 4-(3-bromo-phenyl)-tetrahydro-pyran-4-carboxylic acid methyl ester (610 mg) used in the next step without further purification. LCMS: RT=2.81 minutes; MS: 299, 301 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193183B2
Source datasetuspto-grants-2012_06
ORD IDord-b47f275d210348f18939c95d89aaca09
Source noteuspto-grants-2012_06