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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 14357Generated: October 25, 2026

Ethyl bromoacetate → 14738-27-3

https://huagongshe.com/reaction/14357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
Reactant4-MethylbenzenethiolHCID 7811—
ReactantSodium hydrideHCID 24758—
SolventTetrahydrofuranHCID 8028—
Product14738-27-3HCID 27149299%

Reaction Steps

A solution of 4-methylbenzenethiol (5 g, 40.25) in dry THF was added dropwise to a suspension of NaH (60% in mineral oil, 1.98 g, 48.30) in THF at room temperature and stirred for 30 min. under N2 atmosphere. Ethylbromoacetate (4.9 mL, 44.27) was added slowly to this solution and further stirred at room temperature for 3 h. The solvent was removed under vacuum. The residue was dissolved in dil. HCl and extracted by ethylacetate. The combined organic phase was washed successively with saturated NaHCO3 solution, water and brine then dried over Na2SO4. Evaporation of organic phase yielded 8.46 g (99%) colorless oil. 1H NMR (CDCl3): δ 1.22 (t, J=7.2 Hz, 3H), 2.32 (s, 3H), 3.57 (s, 2H), 4.14 (q, J=7.2 Hz, 2H), 7.11 (d, J=8.0 Hz, 2H), 7.33 (d, J=8.0 Hz, 2H). EIMS m/z 210 (M+1), 233 (M+23).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732146B2
Source datasetuspto-grants-2010_06
ORD IDord-3c2b4df1d7b7494898ee2a0895c03785
Source noteuspto-grants-2010_06