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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2112017생성일: 2026년 10월 26일

Monobenzone → Methyl 2-[(4-{3-[4-(benzyloxy)phenoxy]propyl}phenoxy)methyl]benzoate

https://huagongshe.com/reaction/2112017

반응식

참여 물질

역할이름HCID투입량
반응물MonobenzoneHCID 7638—
반응물CyanomethylenetributylphosphoraneHCID 4622928—
반응물Methyl 2-((4-(3-hydroxypropyl)phenoxy)methyl)benzoateHCID 10780567—
용매TolueneHCID 1140—
생성물Methyl 2-[(4-{3-[4-(benzyloxy)phenoxy]propyl}phenoxy)methyl]benzoateHCID 6886971764.3%

반응 단계

Methyl 2-{[4-(3-hydroxypropyl)phenoxy]methyl}benzoate (0.50 g, 1.66 mmol) and 4-(benzyloxy)phenol (0.33 g, 1.66 mmol) was added to a dry round bottomed flask fitted with a septum Dry toluene (10 ml) was added and N2 was flushed through the mixture for 5 minutes. (Tributylphosphoranylidene)acetonitrile (0.80 g, 3.33 mmol) was added dropwise and the reaction was performed in a single node microwave oven. After removing the solvent 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). Removing the solvent by evaporation gave 0.515 gram of methyl 2-[(4-{3-[4-(benzyloxy)phenoxy]-propyl}phenoxy)methyl]benzoate (yield 64.1%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07521461B2
출처 데이터셋uspto-grants-2009_04
ORD IDord-368ce849ae60442aba721e0c86c78c50
출처 메모uspto-grants-2009_04