HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006736Generated: October 25, 2026
Ethyl 4-bromobutyrate → Ethyl 4-[(3-hydroxypropyl)phenylamino]butanoate
https://huagongshe.com/reaction/1006736
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 4-bromobutyrate | HCID 76300 | — |
| Reactant | 3-(Phenylamino)propan-1-ol | HCID 410467 | — |
| Solvent | Diisopropylethylamine | HCID 81531 | — |
| Product | Ethyl 4-[(3-hydroxypropyl)phenylamino]butanoate | HCID 66716979 | 100.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06790945B2 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-95c11b2babd749d6a794139d62d564b1 |
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| Source note | uspto-grants-2004_09 |
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