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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2112021생성일: 2026년 10월 24일

Dimethyl Sulfide → Methyl 2-({4-[3-(4-hydroxyphenoxy)propyl]phenoxy}methyl)benzoate

https://huagongshe.com/ko/reaction/2112021

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfideHCID 1068—
반응물Boron trifluoride etherateHCID 8000—
반응물Ethyl AcetateHCID 8857—
반응물Methyl 2-[(4-{3-[4-(benzyloxy)phenoxy]propyl}phenoxy)methyl]benzoateHCID 68869717—
용매DichloromethaneHCID 6344—
생성물Methyl 2-({4-[3-(4-hydroxyphenoxy)propyl]phenoxy}methyl)benzoateHCID 6886977657.6%

반응 단계

Methyl 2-[(4-{3-[4-(benzyloxy)phenoxy]propyl}phenoxy)methyl]benzoate (0.70 g, 1.45 mmol) was dissolved in dichloromethane (10 ml). Dimethylsulfide (1.08 g, 17.4 mmol) and boron trifluoride etherate (2.06 g, 14.5 mmol) was added and the mixture was stirred at room temperature for six hours. EtOAc (10 ml) was added and the organic phase was washed with water (3×10 ml), dried (MgSO4) and the solvent was removed by evaporation. The crude was purified by preparative HPLC (started with acetonitrile/buffer 60/40 and then the acetonitrile concentration was increased to 100%, the buffer was a mixture of acetonitrile/water 10/90 and ammonium acetate (0.1 M, column KR-100-7-C8, 50 mm×250 mm, flow 40 ml/min)). The product containing fractions were pooled and the acetonitrile was removed by evaporation. EtOAc (10 ml) was added and the organic phase was washed with two portions of brine and dried (MgSO4). After removing the solvent by evaporation 0.328 gram of methyl 2-({4-[3-(4-hydroxyphenoxy)propyl]-phenoxy}methyl)benzoate (yield 57.6%) was obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07521461B2
출처 데이터셋uspto-grants-2009_04
ORD IDord-eebe9b9ac4ce440d9e8dd79b7425d8e3
출처 메모uspto-grants-2009_04