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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1194768생성일: 2026년 10월 27일

1,3,5-Trithiane → 2-{Bis(4-fluorophenyl)hydroxymethyl}-1,3,5-trithiane

https://huagongshe.com/reaction/1194768

반응식

참여 물질

역할이름HCID투입량
반응물1,3,5-TrithianeHCID 9264—
반응물4,4'-DifluorobenzophenoneHCID 9582—
반응물LithiumHCID 3028194—
용매TetrahydrofuranHCID 8028—
생성물2-{Bis(4-fluorophenyl)hydroxymethyl}-1,3,5-trithianeHCID 1432925883.2%

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-bytyl 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 4.4 g of 4,4'-difluorobenzophenone dissolved in 100 ml of tetrahydrofuran was dropped thereinto. After completion of the dropping, the reaction temperature was slowly raised to 0° C. After stirring at 0° C. for another 1 hour, the reaction mixture thus obtained was poured into ice water and the resulting mixture was extracted with chloroform. The extract was washed with a saturated aqueous sodium chloride solution and then dried over anhydrous magnesium sulfate, and the solvent was removed by distillation under reduced pressure. The crude product thus obtained was recrystallized from ether-hexane to give 5.58 g of the desired compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04816475
출처 데이터셋uspto-grants-1989_03
ORD IDord-2b0b1f81f7bf41a88f7434cf1ae8dfdd
출처 메모uspto-grants-1989_03