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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892685Generated: October 30, 2026

Water → 3-Diethylamino-2,2-diethylpropanol

https://huagongshe.com/reaction/892685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAcetic AnhydrideHCID 7918—
ReactantEthyl 2-{N,N-Diethylcarbamoyl)-2-ethylbutyrateHCID 14987123—
ReactantAluminium lithium hydrideHCID 21226445—
SolventChloroformHCID 6212—
SolventTetrahydrofuranHCID 8028—
Product3-Diethylamino-2,2-diethylpropanolHCID 1498712448.9%

Reaction Steps

To THF (300 ml.) is added LiAlH4 (1.2 g), the mixture is refluxed for 20 min, and an additional quantity of LiAlH4 (15.8 g., 0.42 mole) is added in two portions at 5°-21° over 1 min with mechanical stirring. The mixture is cooled to 5° and a solution of ethyl 2-(N,N-diethylcarbamoyl)-2-ethylbutyrate (29 g., 0.12 mole) in THF (80 ml.) is added at 5°-11° in 5 min. The temperature (exothermic) is allowed to rise to 60° over 12 min, is maintained at 49°-53° for 7 min, is heated gradually to reflux over 10 min, and then is refluxed for 6 hours. After it stands at room temperature for 18 hours, the reaction mixture is treated with Ac2O (55 ml.) at 10°-20° is stirred in an ice bath for 0.5 hour, is treated with H2O (150 ml.) at 10°-18°, and finally is treated with CHCl3 (250 ml.) at 10°-22° with slow stirring. The CHCl3 -layer is washed with H2O (50 ml.), is dried over MgSO4, is filtered, and is concentrated to dryness under reduced pressure. The resultant oil (30 ml.) is treated with 10% HCl (280 ml.) and is subjected to steam distillation for 1.3 hours, collecting 1 liter of distillate. The distillate is concentrated to 50 ml. by distillation under reduced pressure, is made basic with solid NaC2O3 to pH 8-9 in the cold, is extracted with ether, is dried over MgSO4 and activated charcoal, is filtered, and concentrated to dryness. The residual oil (12 g. plus 5.0 g. from previous run) is distilled at 60°-68°/l mm to yield 11 g (35%) of 3-diethylamino-2,2-diethylpropanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05118708
Source datasetuspto-grants-1992_06
ORD IDord-1b7e0e0a337240e9a238ab50a2f087cf
Source noteuspto-grants-1992_06