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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 539512생성일: 2026년 10월 23일

Triethylamine → 4-Ethynylbenzyl methanesulfonate

https://huagongshe.com/ko/reaction/539512

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Methanesulfonyl chlorideHCID 31297—
반응물(4-Ethynylphenyl)methanolHCID 11170993—
용매DichloromethaneHCID 6344—
생성물4-Ethynylbenzyl methanesulfonateHCID 5943577388.1%

반응 단계

To a solution of 4-ethynylbenzyl alcohol (5.0 g, 37.8 mmol) in CH2Cl2 (50 mL) and triethylamine (Et3N) (14.4 mL, 104.0 mmol) was added mesyl chloride (8.04 mL, 104.0 mmol) at 0° C. and the reaction was allowed to warm to room temperature. Stirring continued for 2 h under argon during which TLC revealed a quantitative conversion into a higher Rf product. Ice cold water was added into the reaction mixture and extracted with Et2O (200 ml). The organic layer was washed with 1N HCL (70 ml), H2O (100 ml), aqueous NaHCO3 (70 ml), and finally H2O (100 ml); and then dried over Na2SO4. Solvent was evaporated off and dried in vacuo to give 7.0 g of compound 3 as brownish oil which was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08871728B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-083069f06696482fb8af521dee74d4d7
출처 메모uspto-grants-2014_10