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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1395생성일: 2026년 10월 23일

Tetrabutylammonium Fluoride → 4-([(5,5-Dimethyl-5,6-dihydro-8-(2-thienyl)-naphthalen-2-yl)carbonyl]oxy]-benzoic acid

https://huagongshe.com/ko/reaction/1395

반응식

참여 물질

역할이름HCID투입량
반응물Tetrabutylammonium FluorideHCID 2724141—
반응물2-Trimethylsilylethyl 4-[[(5,5-dimethyl-5,6-dihydro-8-(2-thienyl)-naphthalen-2-yl)carbonyl]oxy]-benzoateHCID 10601629—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물4-([(5,5-Dimethyl-5,6-dihydro-8-(2-thienyl)-naphthalen-2-yl)carbonyl]oxy]-benzoic acidHCID 9953061—

반응 단계

To a solution of 2-trimethylsilylethyl 4-[[(5,5-dimethyl-5,6-dihydro-8-(2-thienyl)-naphthalen-2-yl)carbonyl]oxy]-benzoate (Compound E10, 100.0 mg, 0.198 mmol) in 2.0 mL THF at room temperature was added 155.3 mg of tetrabutylammonium fluoride (0.594 mmol 0.6 mL of a 1M solution in THF). After stirring overnight the reaction was diluted with EtOAc and washed with H2O and saturated aqueous NaCl before being dried over MgSO4. The solvents were removed under reduced pressure and the residue washed with hot acetonitrile leaving the product as a colorless solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723666
출처 데이터셋uspto-grants-1998_03
ORD IDord-54921a0488e14a3e81bfab9c9a8565e8
출처 메모uspto-grants-1998_03