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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 435425생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/435425

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylamineHCID 7912—
반응물CyclohexaneHCID 8078—
반응물3-Methyl-2-butenenitrileHCID 94301—
반응물1-(Isopropylsulfonyl)-4-methylbenzeneHCID 816792—
반응물Monosodium phosphateHCID 23672064—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물4-p-Tolylsulfonyl-4,3,3,-trimethyl-pentanenitrileHCID 12833028—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04401601
출처 데이터셋uspto-grants-1983_08
ORD IDord-65212fa3874a4fbfb05ef8243326a26e
출처 메모uspto-grants-1983_08