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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029500Generated: November 1, 2026

Diisopropylamine → Ethyl 4-diisopropylaminobutyrate

https://huagongshe.com/reaction/1029500

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantEthyl 4-bromobutyrateHCID 76300—
SolventEthanolHCID 702—
ProductEthyl 4-diisopropylaminobutyrateHCID 1990043321.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05102890
Source datasetuspto-grants-1992_04
ORD IDord-c80d78822dce493db7d88a0ee234263e
Source noteuspto-grants-1992_04