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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654333Generated: November 2, 2026

Ethyl Bromide → HCID 15506059, compound

https://huagongshe.com/reaction/1654333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 3-HydroxyphenylacetateHCID 39129—
SolventDimethylformamideHCID 6228—
ProductHCID 15506059HCID 1550605961.1%

Reaction Steps

Methyl 3-hydroxyphenylacetate (132.5 g, 0.80 mole) was added dropwise to a suspension of 50% NaH (43.2 g, 0.90 mole) in DMF (ie) at 0° C. under N2. The solution was stirred 1 hour at room temperature, cooled in an ice bath, and ethyl bromide (120 ml, 1.6 mole) added. The reaction mixture was stirred overnight at room temperature, filtered, and concentrated in vacuo. A solution of the residue in diethyl ether was washed with dilute NaOH solution and saturated NaCl, dried (Na2SO4) and concentrated in vacuo. The residue was purified by chromatography on silica gel eluting with ethyl acetate: hexane (1:39→1:9) to give methyl 3-ethoxyphenylacetate (94.9 g). 1H NMR (DMSO-d6, 200 MHz) δ: 1.30 (t, J=7 Hz, 3H, ethyl CH3), 3.59 (s, 3H, ester CH3), 3.61 (s, 2H, ArCH2), 3.98 (q, J=7 Hz, 2H, ethyl CH2), 6.78-6.81 (m, 3H), 7.16-7.24 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05405851
Source datasetuspto-grants-1995_04
ORD IDord-e1742c29bc4440b2ae0df4852544d524
Source noteuspto-grants-1995_04