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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 381541Generated: October 31, 2026

Ethyl Bromide → HCID 15506059, compound

https://huagongshe.com/reaction/381541

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, 2B, ethyl CH2), 6.78-6.81 (m, 3H), 7.16-7.24 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06306865B1
Source datasetuspto-grants-2001_10
ORD IDord-ea94a363ab3f4c22a0b87d02d5fd9daa
Source noteuspto-grants-2001_10