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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2112018생성일: 2026년 10월 26일

Hydrochloric Acid → 2-[(4{3-[4-(Benzyloxy)phenoxy]propyl}phenoxy)methyl]-benzoic acid

https://huagongshe.com/reaction/2112018

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Lithium HydroxideHCID 3939—
반응물Methyl 2-[(4-{3-[4-(benzyloxy)phenoxy]propyl}phenoxy)methyl]benzoateHCID 68869717—
용매Oxolane--water (1/1)HCID 21881883—
생성물2-[(4{3-[4-(Benzyloxy)phenoxy]propyl}phenoxy)methyl]-benzoic acidHCID 104123374.4%

반응 단계

Methyl 2-[(4-{3-[4-(benzyloxy)phenoxy]propyl}phenoxy)methyl]benzoate (0.047 g, 0.097 mmol) was dissolved in a mixture of THF/water (7/1, 2 ml) and lithium hydroxide (9.3 mg, 0.39 mmol) was added. The reaction was performed in a single node microwave oven (7 min, 150° C.). The reaction mixture was acidified (HCl, 1 M, 1 ml) and the water phase was washed with two portions of EtOAc (2×5 ml). The organic phases were combined, dried (MgSO4) and the solvent was removed by evaporation. The crude product 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 2 mg of 2-[(4{3-[4-(benzyloxy)phenoxy]propyl}phenoxy)methyl]-benzoic acid (yield 4.4%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07521461B2
출처 데이터셋uspto-grants-2009_04
ORD IDord-83b71f0b6f9e45088ae3dc02e782bc29
출처 메모uspto-grants-2009_04