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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2179932생성일: 2026년 10월 27일

Ethyl methyl sulfide → 3-Phenyl-2-prop-2-ynylamino-propionic acid methyl ester

https://huagongshe.com/reaction/2179932

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl methyl sulfideHCID 12230—
반응물2-[(4-Methoxy-2,3,6-trimethyl-benzenesulfonyl)-prop-2-ynyl-amino]-3-phenyl-propionic acid methyl esterHCID 20779306—
용매1,1-DichloroethaneHCID 6365—
용매Trifluoroacetic acidHCID 6422—
생성물3-Phenyl-2-prop-2-ynylamino-propionic acid methyl esterHCID 20779308—

반응 단계

To a solution of 2-[(4-Methoxy-2,3,6-trimethyl-benzenesulfonyl)-prop-2-ynyl-amino]-3-phenyl-propionic acid methyl ester (150 mg, 0.349 mmol) in anhydrous dichloroethane (1.5 mL), trifluoroacetic acid (3.5 mL) and ethyl methyl sulfide (0.16 mL, 1.75 mmol) were added. The reaction mixture was stirred at room temperature under a N2 atmosphere for 12 h. Excess of solvents were removed under reduced pressure and the residue was extracted between saturated NaHCO3 solution and ethyl acetate. The organic layer was separated, dried (Na2SO4), concentrated. The crude product was purified by silica gel column chromatography using ethyl acetate and hexane (1:3) as eluent to obtain 3-Phenyl-2-prop-2-ynylamino-propionic acid methyl ester as a thick syrup, 70 mg (92%). 1H NMR (CDCl3, 400 MHz): δ7.32-7.19 (m, 5H), 3.78 (t, 1H), 3.68 (s, 3H), 3.40 (ABq, 2H), 3.03 (dd, 1H), 2.98 (dd, 1H), 1.99 (t, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06887877B2
출처 데이터셋uspto-grants-2005_05
ORD IDord-14d2abf5250847349088d3c5a01ad3f0
출처 메모uspto-grants-2005_05