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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2223010생성일: 2026년 10월 25일

4-Toluenesulfonyl chloride → 5-Tosyloxymethyl-1,3-oxazolidine-2-one

https://huagongshe.com/reaction/2223010

반응식

참여 물질

역할이름HCID투입량
반응물4-Toluenesulfonyl chlorideHCID 7397—
반응물TriethylamineHCID 8471—
반응물5-(Hydroxymethyl)oxazolidin-2-oneHCID 10290773—
용매DichloromethaneHCID 6344—
생성물5-Tosyloxymethyl-1,3-oxazolidine-2-oneHCID 279376980%

반응 단계

p-Toluenesulphonyl chloride (2.74 g, 14.36 mmol) and Et3N (1.45 g, 14.36 mmol) were added to 5-hydroxymethyl-1,3-oxazolidine-2-one (1.40 g, 11.97 mmol) dispersed in 20 mL of dichloromethane and stirred overnight at room temperature under N2. After completion of the reaction (TLC), the solvent in the reaction mixture was evaporated and the residue was purified by column chromatography employing EtOAc-hexane (70:30) as eluent to afford 5-tosyloxymethyl-1,3-oxazolidine-2-one in 80% yield. m.p. 96-99° C.; [α]27D=+45.40 CHCl3); IR (KBr) 3302, 2980, 2925, 2871, 1757, 1694, 1357, 1184, 1090, 996, 965 cm1; 1HNMR (200 MHz, CDCl3) δ 2.47 (s, 3H), 3.40-3.50 (m, 1H), 3.64-3.74 (m, 1H), 4.14 (d, 2H, J=4.4 Hz), 4.71-4.82 (m, 1H), 7.35 (d, 2H, J=8.2 Hz), 7.78 (d, 2H, J=8.2 Hz); Mass (EI) 271, 207, 173, 155, 139, 91.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07374926B2
출처 데이터셋uspto-grants-2008_05
ORD IDord-ee0f40122a1f4cb58afa3bf550f298a1
출처 메모uspto-grants-2008_05