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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114593Generated: October 31, 2026

Ethyl bromoacetate → 14738-27-3

https://huagongshe.com/reaction/2114593

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 numberUS07435737B2
Source datasetuspto-grants-2008_10
ORD IDord-5acf1a5f4f384895b7853ae3b25b9be8
Source noteuspto-grants-2008_10