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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 41071생성일: 2026년 10월 23일

1,2-Dichloroethane → (S)-tert-butyl 3-((R)-2-(pent-4-enoyloxy)-2-phenylethylcarbamoyl)hex-5-enoate

https://huagongshe.com/ko/reaction/41071

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물4-Pentenoic acidHCID 61138—
반응물DiisopropylethylamineHCID 81531—
반응물(S)-tert-butyl 3-((R)-2-hydroxy-2-phenylethylcarbamoyl)hex-5-enoateHCID 67312340—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DimethylformamideHCID 6228—
생성물(S)-tert-butyl 3-((R)-2-(pent-4-enoyloxy)-2-phenylethylcarbamoyl)hex-5-enoateHCID 6731075174%

반응 단계

To a solution of 4-pentenoic acid (0.335 mL, 3.28 mmol) in DMF (31.6 mL) cooled in an ice/water bath was added EDC (630 mg, 3.28 mmol) and the resulting solution was stirred 30 min. (S)-tert-butyl 3-((R)-2-hydroxy-2-phenylethylcarbamoyl)hex-5-enoate (730 mg, 2.19 mmol), iPr2NEt (1.14 mL, 6.57 mmol) and DMAP (26.7 mg, 0.219 mmol) were subsequently added and the reaction mixture was slowly warmed to rt and stirred for 16 h at which point LC-MS analysis indicated complete consumption of starting material. The reaction mixture was diluted with saturated NH4Cl and EtOAc and the layers separated. The aqueous was extracted 2× with EtOAc and the combined organic extracts were washed with 1N HCl and brine, dried over Na2SO4, filtered, and concentrated. The crude product was purified using silica gel chromatography (MeOH/CH2Cl2 gradient) to yield 670 mg of desired product as a colorless oil in 74% yield. LRMS (M+Na)+: 430.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530456B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-4b3c48075aa44cf38924fdf68a33a632
출처 메모uspto-grants-2013_09