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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1393412Generated: November 3, 2026

4-tert-Butylphenol → Ethyl 2-(4-tert-butylphenoxy)propanoate

https://huagongshe.com/reaction/1393412

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-ButylphenolHCID 7393—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 2-bromopropionateHCID 79040—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductEthyl 2-(4-tert-butylphenoxy)propanoateHCID 3023318100%

Reaction Steps

4-t-Butylphenol (7.52 g, 50 mmol) in anhydrous DMF (40 mL) was added dropwise to NaH (2.2 g, 55 mmol, 60% w/w in mineral oil) at 0° C. under an atmosphere of nitrogen. After five min, ethyl 2-bromopropionate (6.49 mL, 50 mmol, d=1.394) was added rapidly dropwise and the resultant mixture was allowed to stir for 18 h, gradually warming to ambient temperature. The reaction mixture was diluted with ethyl acetate (300 mL) and extracted twice with water and once with brine. The organic layer was dried over Na2SO4 and concentrated in vacuo to produce a colorless oil (12.5 g, 100%) 1H NMR (300 MHz, CDCl3): δ 7.28 (d, 2H, J=5.5), 6.80 (d, 2H, J=5.5), 4.70 (q, 1H, J=6.6), 4.22 (q, 2H, J=7.1), 1.59 (d, 3H, J=6.6), 1.28 (s, 9H), 1.25 (t, 3H, J=7.1). MS [EI+] 251 (M+H)+, 268 (M+NH4)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07345070B2
Source datasetuspto-grants-2008_03
ORD IDord-2ee87feefcb74c2d803231ede5834bf6
Source noteuspto-grants-2008_03