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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2242787Generated: November 2, 2026

Diisopropylamine → HCID 68743244, compound

https://huagongshe.com/reaction/2242787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantChloromethyl ethyl etherHCID 18523—
ReactantLithium diisopropylamideHCID 2724682—
ReactantHCID 68744317HCID 68744317—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68743244HCID 6874324464.3%

Reaction Steps

A solution of lithium diisopropylamide prepared from diisopropylamine (6.50 mL) and butyllithium (29.0 mL of 1.6M solution in hexanes) in THF (105 mL) was treated dropwise with 2-(cyclohexyl-methyl)-γ-butyrolactone (6.96 g) at −78° C. The reaction mixture was stirred at the same temperature for additional 30 min and then treated dropwise with chloromethyl ethyl ether (5.05 g). Upon completion of the addition, the mixture was allowed to slowly warm-up to room temperature and stirred at this temperature overnight. After that, the mixture was quenched by pouring onto a mixture of ice and 10% aqueous phosphoric acid. The formed organic phase was separated and the aqueous phase was extracted with toluene. The combined organic phases were washed with water, dried over potassium sulfate, filtered, concentrated on a rotary evaporator and purified by column chromatography (silica gel, eluent-hexane) to give 5.90 g (64%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674741B2
Source datasetuspto-grants-2010_03
ORD IDord-52da25c55cf6475287b7e8a38face0c8
Source noteuspto-grants-2010_03