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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1769804Generated: October 30, 2026

Diisopropylamine → HCID 20097372, compound

https://huagongshe.com/reaction/1769804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantHexaneHCID 8058—
ReactantN-Ethylidene-2-methylpropan-2-amineHCID 138901—
ReactantMethanone, (2,6-dimethoxyphenyl)phenyl-HCID 872417—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20097372HCID 2009737294%

Reaction Steps

A solution of diisopropylamine (10.1 g, 0.1 mol) in dry ether (100 ml) was cooled to -10°. A solution of butyl lithium in hexane (65 ml, 0.1 mol) was added, and the mixture was stirred at -10° for 20 min. A solution of N-ethylidene-tert.butylamine (10 g, 0.1 mol) in dry ether (100 ml) was added and the solution was stirred at 0° for 20 min. After cooling to -30° a solution of 2,6-dimethoxybenzophenone (24.1 g, 0.1 mol) in dry ether (100 ml), containing 30 ml THF, was added. The mixture was then stirred at ambient temperature for 20 h and hydrolized with water. The organic phase was washed with water, dried and evaporated, giving 32 g (94%) of N-(3-(2,6-dimethoxyphenyl)-3-hydroxy-3phenylpropylidene)tert.butylamine as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05382600
Source datasetuspto-grants-1995_01
ORD IDord-be896e615eaf408c97a14da6c7d37bc6
Source noteuspto-grants-1995_01