돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 47716생성일: 2026년 10월 25일

Water → ethyl (2R)-2-(acetylamino)-3-(3-thienyl)propanoate

https://huagongshe.com/reaction/47716

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Ammonium BicarbonateHCID 14013—
반응물Ethyl 2-acetamido-3-(thiophen-3-yl)propanoateHCID 22747902—
용매AcetonitrileHCID 6342—
생성물ethyl (2R)-2-(acetylamino)-3-(3-thienyl)propanoateHCID 8658442345.6%

반응 단계

3.95 g of ammonium hydrogen carbonate and 35 cm3 of deionized water are added to a stirred solution, under an inert atmosphere, of 2.41 g of ethyl 2-(acetylamino)-3-(3-thienyl)propanoate in 17 cm3 of acetonitrile. 0.017 g of type-II α-chymotrypsin is added and the pH of the reaction medium is then in the region of 8. This mixture is stirred for 1 hour at room temperature and, after checking that the pH is still at 8, a further 0.017 g of type-II α-chymotrypsin is added. After stirring for 1 hour, with the pH remaining constant, a further 0.017 g of type-II α-chymotrypsin is introduced and stirring of the reaction mixture is continued for 19 hours at room temperature. The acetonitrile is evaporated off under reduced pressure (2 kPa) at a temperature in the region of 33° C. and 25 cm3 of ethyl acetate are then added to the residual aqueous phase. The emulsion obtained is filtered through Celite and the aqueous phase is then extracted with twice 25 cm3 of ethyl acetate. The organic phases are combined, washed with twice 15 cm3 of sodium carbonate solution and then evaporated under reduced pressure (2 kPa) at a temperature in the region of 40° C. The solid residue is then dried in an oven under vacuum (10 Pa) at room temperature. 1.1 g of ethyl (2R)-2-(acetylamino)-3-(3-thienyl)propanoate are obtained in the form of a beige-colored solid melting at about 75° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06699895B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-336d168da36a4264891a3782c0be6f9b
출처 메모uspto-grants-2004_03