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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480289Generated: October 26, 2026

Diethyl Ether → Ethyl 2-(4-bromobutoxy)acetate

https://huagongshe.com/reaction/480289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant1,4-DibromobutaneHCID 8056—
ReactantEthyl GlycolateHCID 12184—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductEthyl 2-(4-bromobutoxy)acetateHCID 2043684317.7%

Reaction Steps

A solution of ethyl glycolate (4.6 g, 44 mmol) in DMF (50 mL) was cooled to 0° C. and′ sodium bis(trimethylsilyl)amide (1.0 M in THF, 53 mL, 53 mmol) was slowly added. The reaction was stirred for 15 minutes and 1,4-dibromobutane (5.6 mL, 48.4 mmol) was added. The reaction was warmed to room temperature and was stirred for 24 h. Et2O was added, and the organic solution was washed consecutively with HCl (1N, 3×), water (3×), and brine (1×). The organic solution was dried (Na2SO4), filtered, and concentrated. Attempted vacuum distillation removed a majority of the impurities and provided a mixture of product and 1,4-dibromobutane (3.539 g). Flash chromatography (9:1 hexanes:EtOAc) of this material provided (4-bromo-butoxy)-acetic acid ethyl ester (1.862 g). 1H NMR (400 MHz, CDCl3) δ 4.19 (q, 2H), 4.04 (s, 2H), 3.54 (t, 2H), 3.45 (t, 2H), 1.97 (m, 2H), 1.75 (m, 2H), 1.26 (t, 3H); MS 239.1 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06649657B2
Source datasetuspto-grants-2003_11
ORD IDord-9fc26ce195e046b585ab65c58fed5c93
Source noteuspto-grants-2003_11