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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 536738생성일: 2026년 10월 24일

4-Toluenesulfonyl chloride → Cyclobutylmethyl 4-methylbenzenesulfonate

https://huagongshe.com/ko/reaction/536738

반응식

참여 물질

역할이름HCID투입량
반응물4-Toluenesulfonyl chlorideHCID 7397—
반응물CyclobutylcarbinolHCID 78130—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매PyridineHCID 1049—
용매DichloromethaneHCID 6344—
생성물Cyclobutylmethyl 4-methylbenzenesulfonateHCID 1316393173%

반응 단계

To a solution of cyclobutylmethanol (25 g, 290 mmol) in CH2Cl2 (200 mL) and pyridine (100 mL) was added 4-(dimethylamino)pyridine (1.8 g, 14.5 mmol) followed by p-toluenesulfonyl chloride (55.3 g, 290 mmol). The mixture was allowed to stir at ambient temperature for 20 hours then quenched with 5% aqueous HCl (30 mL). The layers were separated and the aqueous phase was extracted with CH2Cl2 (3×15 mL). The combined organic extracts were dried over Na2SO4, filtered and concentrated under reduced pressure. Purification by column chromatography (SiO2, 75% hexanes in EtOAc) afforded the title compound (50.8 g, 211 mmol, 73% yield). MS (DCI/NH3) m/z 258 (M+NH4)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08859596B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-53306f91990749859c5bdde3186e8017
출처 메모uspto-grants-2014_10