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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 248178생성일: 2026년 10월 24일

Benzyl Chloride → alpha-Methyl-6-(phenylmethoxy)-2-naphthaleneacetic acid

https://huagongshe.com/ko/reaction/248178

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl ChlorideHCID 7503—
반응물DesmethylnaproxenHCID 162920—
반응물Sodium MethoxideHCID 10942334—
용매MethanolHCID 887—
생성물alpha-Methyl-6-(phenylmethoxy)-2-naphthaleneacetic acidHCID 1503017738.1%

반응 단계

To a solution of 6-hydroxy-α-methyl-2-naphthaleneacetic acid (6.48 g, 30 mmol) in methanol (100 ml) is added sodium methoxide (60 mmol). After 10 minutes the solvent is removed and replaced with dimethylformamide (100 ml). Benzyl chloride (7.6 g, 60 mmol) is then added and the reaction mixture is stirred overnight at room temperature. The reaction is then heated at 150° C. for 1 hour. The solvent is then removed and the residue is partitioned between water and methylene chloride. The organic layer is washed with water, dried over magnesium sulfate and evaporated to 11.5 g of crude product. This crude product is extracted with 100 ml hot hexane which affords 3.5 g of white crystals. A final recrystallization from methanol affords 2.5 g of white crystals of the intermediate ether ester (21% yield, m.p. 76°-78° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05208344
출처 데이터셋uspto-grants-1993_05
ORD IDord-a87f303f0be841629e4d49b56aa519a5
출처 메모uspto-grants-1993_05