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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 638105생성일: 2026년 10월 27일

Ethyl Methanesulfonate → 2-Phenylbutyric Acid

https://huagongshe.com/reaction/638105

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl MethanesulfonateHCID 6113—
반응물Methyl phenylacetateHCID 7559—
반응물Ammonium ChlorideHCID 25517—
촉매PlatinumHCID 23939—
촉매Tetraethylammonium p-toluenesulphonateHCID 101846—
용매DimethylformamideHCID 6228—
생성물2-Phenylbutyric AcidHCID 7012—
생성물Benzeneacetic acid, alpha-ethyl-, methyl esterHCID 102780—

반응 단계

Into the cathode chamber of an electrolytic cell divided with an ion-exchange resin diaphragm was placed a solution of 10 mmols of methyl phenylacetate, 12 mmols of ethyl methanesulfonate and 1.0 g of tetraethylammonium tosylate in 30 ml of anhydrous dimethylformamide. And the anode chamber was provided with a solution of 1.0 g of tetraethylammonium tosylate in 10 ml of anhydrous dimethylformamide. Constant current electrolysis was performed at 0.2 A/cm2 with use of platinum for the cathode and carbon for the anode. After passing 1.5 F of electricity per mol of the methyl phenylacetate through the solution at 5 to 10 C, the cathode solution was added to a saturated aqueous solution of ammonium chloride and the mixture was extracted twice with ether. The ether was distilled off and the residue was purified by silica gel column chromatography using hexane-ethyl acetate (10:1), giving methyl α-ethylphenylacetate in a yield of 77% and α-ethylphenylacetic acid in a yield of 13%. The spectral data of the ester were as follows.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04560447
출처 데이터셋uspto-grants-1985_12
ORD IDord-3c500045094e49f49dab1007d63f00e8
출처 메모uspto-grants-1985_12