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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2941생성일: 2026년 10월 24일

Hydrochloric Acid → 5-[[3,5-Bis(1,1-dimethylethyl)-4-hydroxyphenyl]methylene]-3-ethyl-4-thiazolidinone

https://huagongshe.com/ko/reaction/2941

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물IodoethaneHCID 6340—
반응물Sodium hydrideHCID 24758—
반응물5-(3,5-Bis(tert-butyl)-4-hydroxyphenyl)methylene-4-thiazolidinoneHCID 130003—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물5-[[3,5-Bis(1,1-dimethylethyl)-4-hydroxyphenyl]methylene]-3-ethyl-4-thiazolidinoneHCID 53773360—

반응 단계

To a solution of 9.58 g of 5-[[3,5-bis(1,1-dimethylethyl) -4-hydroxyphenyl]methylene]-4-thiazolidinone in 150 ml of tetrahydrofuran were added 1.20 g of a 60% dispersion of sodium hydride in mineral oil. After gas evolution ceased, 2.4 ml of ethyl iodide were added and the reaction mixture was stirred for two days under an argon atmosphere. The mixture was heated at reflux for six hours, cooled, diluted with diethyl ether and water, and adjusted to pH 3 with 1N hydrochloric acid. The layers were separated, and the organic layer was washed with a saturated sodium bicarbonate solution followed by a saturated sodium chloride solution. Concentration of the dried organic solution and chromatography of the resulting residue over silica gel eluting with a 10-30% ethyl acetate in hexane gradient provided 3.65 g of the desired title product, m.p. 169°-172.5° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05731336
출처 데이터셋uspto-grants-1998_03
ORD IDord-99da04be27454cd9bffd7d2ff5f26253
출처 메모uspto-grants-1998_03