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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435425Generated: October 25, 2026

Diisopropylamine → 4-p-Tolylsulfonyl-4,3,3,-trimethyl-pentanenitrile

https://huagongshe.com/reaction/435425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantCyclohexaneHCID 8078—
Reactant3-Methyl-2-butenenitrileHCID 94301—
Reactant1-(Isopropylsulfonyl)-4-methylbenzeneHCID 816792—
ReactantMonosodium phosphateHCID 23672064—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product4-p-Tolylsulfonyl-4,3,3,-trimethyl-pentanenitrileHCID 12833028—

Reaction Steps

3.81 ml of a cyclohexane solution of 1.75M of butyllithium were added at -30° to -40° C. to a mixture of 1.05 ml of diisopropylamine and 4 ml of tetrahydrofuran and the mixture was stirred for 10 minutes and was then cooled to -60° to -70° C. Then 1.22 g of p-tolyl isopropylsulfone were added to the mixture which after 15 minutes of contact was poured over 10 minutes under an inert atmosphere into a solution of 0.5 g of dimethylacrylonitrile and 4 ml of tetrahydrofuran at -60° to -70° C. The mixture was stirred for 30 minutes at -60° to -70° C. and was then poured into an aqueous saturated monosodium phosphate solution. The mixture was extracted with benzene and the organic phase was dried and evaporated to dryness. The residue was crystallized from isopropyl ether to obtain 0.740 g of 4-p-tolylsulfonyl-4,3,3,-trimethyl-pentanenitrile melting at 126° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04401601
Source datasetuspto-grants-1983_08
ORD IDord-65212fa3874a4fbfb05ef8243326a26e
Source noteuspto-grants-1983_08