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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444780Generated: October 25, 2026

Ethyl 4-bromobutyrate → Ethyl 4-[(3-hydroxypropyl)phenylamino]butanoate

https://huagongshe.com/reaction/1444780

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-bromobutyrateHCID 76300—
Reactant3-(Phenylamino)propan-1-olHCID 410467—
SolventDiisopropylethylamineHCID 81531—
ProductEthyl 4-[(3-hydroxypropyl)phenylamino]butanoateHCID 66716979100.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 3-(phenylamino)propan-1-ol (Huang et al., J. Org. Chem.; 58(23):6235-6246(1993)) (65.6 g, 0.43 mol), ethyl 4-bromobutyrate (104.5 g, 0.54 mol) and 100 mL of ethyldiisopropylamine is stirred at 100° C. for 1 h. The reaction is cooled to room temperature and partitioned between water 400 mL and ethyl acetate (500 mL). The organic layer is washed with saturated NaHCO3, brine and dried over Na2SO4. The oil obtained after concentration is chromatographed on silica eluting with 10% EtOH/CHCl3. Concentration of the appropriate fractions affords 115 g (100%) of the desired product as a colorless, viscous oil. 1H NMR (CDCl3) δ 7.23 (m, 2H), 6.72 (m, 3H), 4.14 (q, J=7 Hz, 2H), 3.72 (t, J=6 Hz, 2H), 3.43 (t, 7 Hz, 2H), 3.34 (t, 7 Hz, 2H), 2.35 (t, 7 Hz), 1.88 (m, 4H), 1.26 (t, 7 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662942B2
Source datasetuspto-grants-2010_02
ORD IDord-98895fed956f4d6cb1addb10ef41c615
Source noteuspto-grants-2010_02