돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18684생성일: 2026년 10월 24일

Hydrochloric Acid → 2-Butyl-3-(4-iodobenzyl)-1,3-diazaspiro[4.4]non-1-en-4-one

https://huagongshe.com/ko/reaction/18684

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Potassium HydroxideHCID 14797—
반응물4-Iodobenzyl bromideHCID 954258—
반응물2-Butyl-1,3-diazaspiro[4.4]non-1-en-4-oneHCID 10176511—
촉매Tetrabutylammonium hydrogen sulfateHCID 94433—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물2-Butyl-3-(4-iodobenzyl)-1,3-diazaspiro[4.4]non-1-en-4-oneHCID 1199642688%

반응 조건

온도25 °C

반응 단계

A solution of 23.07 g (100 mmol) of the hydrochloride of 2-butyl-1,3-diazaspiro[4,4]non-1-en-4-one and 19.8 g of potassium hydroxide in 100 mL de water is added to a solution of 29.7 g (100 mmol) of 4-iodobenzyl bromide and 3.4 g (10 mmol) of tetrabutylammonium bisulphate in 30 mL of toluene, and the mixture is heated at reflux for 1 hr. After cooling to 25° C., 100 mL of water is added and the phases are separated. To the organic phase is added 10 mL of concentrated hydrochloric acid, 100 mL is evaporated at reduced pressure, 300 mL of ethyl acetate is added and the resulting solid is filtered to give 39.6 g (88%) of the title compound in the form of hydrochloride.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741492B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-cfa93898b13c4cddbdf0bab68e95b661
출처 메모uspto-grants-2010_06