HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029500Generated: November 1, 2026
Diisopropylamine → Ethyl 4-diisopropylaminobutyrate
https://huagongshe.com/reaction/1029500
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Ethyl 4-bromobutyrate | HCID 76300 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 4-diisopropylaminobutyrate | HCID 19900433 | 21.4% |
Reaction Steps
Ethyl 4-diisopropylaminobutyrate may be obtained in the following manner: diisopropylamine (40.4 g) is added dropwise to a solution of ethyl 4-bromobutyrate (39 g) in ethanol (80 cc). The solution obtained is heated to reflux for 6 hours. After the insoluble material formed has been filtered off, the filtrate is concentrated to dryness under reduced pressure (2.7 kPa). The residue is taken up with distilled water (15 cc) and 4 N aqueous hydrochloric acid solution (100 cc). The aqueous phase is washed with ethyl ether (3×75 cc) and then alkalinized with 10 N aqueous sodium hydroxide solution. The oil formed is extracted with ethyl ether (3×75 cc). The organic phase obtained is concentrated to dryness under reduced pressure (2.7 kPa). Ethyl 4-diisopropylaminobutyrate (9.2 g) is thereby obtained in the form of an oil, which is employed in the crude state in the subsequent syntheses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05102890 |
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| Source dataset | uspto-grants-1992_04 |
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| ORD ID | ord-c80d78822dce493db7d88a0ee234263e |
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| Source note | uspto-grants-1992_04 |
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