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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 85118생성일: 2026년 10월 24일

4-Toluenesulfonyl chloride → 2,2-Dimethyl-1,3-dioxolan-4-ylmethyl p-toluenesulfonate

https://huagongshe.com/ko/reaction/85118

반응식

참여 물질

역할이름HCID투입량
반응물4-Toluenesulfonyl chlorideHCID 7397—
반응물SolketalHCID 7528—
반응물TriethylamineHCID 8471—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DichloromethaneHCID 6344—
생성물2,2-Dimethyl-1,3-dioxolan-4-ylmethyl p-toluenesulfonateHCID 235097—

반응 단계

(2,2-Dimethyl-1,3-dioxolan-4-yl)methanol (33; 7.56 mmol, 1.0 g) was taken up in 20 mL of dichloromethane. Triethylamine (26.46 mmol, 3.687 mL) was then added, followed by p-toluensulfonyl chloride (15.12 mmol, 2.88 g) and catalytic amount of 4-dimethylamino pyridine. The reaction was allowed to stir at room temperature for 18 h. The crude reaction mixture was diluted with dichloromethane, washed successively with saturated aqueous sodium bicarbonate solution, water, dried (Na2SO4) and concentrated under reduced pressure. The resulting residue 34 was used for the next step without further purification (89% crude yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846947B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-ac5e6c1e7fdd4b0881b08a7d39fef9a6
출처 메모uspto-grants-2014_09