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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481174Generated: October 25, 2026

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

https://huagongshe.com/reaction/481174

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) δ7.23 (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 numberUS06653473B2
Source datasetuspto-grants-2003_11
ORD IDord-1d46b4bfd06d4876812e01d0fc3990c8
Source noteuspto-grants-2003_11