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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 727862생성일: 2026년 10월 24일

1,3,5-Trithiane → 2-{1-(4-Phenoxyphenyl)-1-hydroxyethan-1-yl}-1,3,5-trithiane

https://huagongshe.com/ko/reaction/727862

반응식

참여 물질

역할이름HCID투입량
반응물1,3,5-TrithianeHCID 9264—
반응물4'-PhenoxyacetophenoneHCID 236783—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물2-{1-(4-Phenoxyphenyl)-1-hydroxyethan-1-yl}-1,3,5-trithianeHCID 1432926870%

반응 조건

온도-60 °C

반응 단계

In 30 ml of anhydrous tetrahydrofuran was suspended 2.6 g of 1,3,5-trithiane, and 12 ml of 1.6M n-butyl lithium was added dropwise under an argon atmosphere at a temperature of about -20° C. After completion of the dropwise addition, the resulting mixture was stirred for 2 hours. Next, the reaction mixture was cooled to about -60° C., and then a solution of 4.0 g of 4-phenoxyacetophenone dissolved in 10 ml of tetrahydrofuran was dropped thereinto. After completion of the dropping, the reaction temperature was slowly raised to 0° C. The mixture thus obtained was stirred at 0° C. for another 1 hour. Thereafter, the same treatment as in Example 1 was carried out to obtain a crude product, which was then purified by a silica gel column chromatography (chloroform) to give 3.4 g of the desired compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05045562
출처 데이터셋uspto-grants-1991_09
ORD IDord-16ba98998bca43b5b108e5d9646c706c
출처 메모uspto-grants-1991_09