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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1600525생성일: 2026년 10월 24일

Hydrochloric Acid → Boc-homophenylalaninal

https://huagongshe.com/ko/reaction/1600525

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물4-MethylmorpholineHCID 7972—
반응물Isobutyl chloroformateHCID 62365—
반응물CP 84364HCID 664657—
반응물ethyl (S)-4-amino-6-phenyl-2-hexenoate hydrochlorideHCID 86754733—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
생성물Boc-homophenylalaninalHCID 1026474080%

반응 단계

Morpholinecarbonylphenylalanine (2.74 g, 9.82 mmol, prepared according to the method described in Esser, R. et.al., Arthritis & Rheumatism (1994), 0000) was dissolved in THF (50 mL) at -10° C. 4-methylmorpholine (1.08 mL, 9.82 mmol) was added, followed by isobutyl chloroformate (1.27 mL, 9.82 mmol). The mixed anhydride was stirred for 10 minutes, whereupon a solution of ethyl (S)-4-amino-6-phenyl-2-hexenoate hydrochloride from the previous step in DMF (10 mL) was added, followed by 4-methylmorpholine (1.08 mL, 9.82 mmol). The mixture was stirred for 1 hour. 1M HCl (50 mL) was added. The product was extracted with ethyl acetate (100 mL), washed with saturated aqueous NaHCO3 (50 mL), dried over MgSO4 and decolorizing charcoal (DARCO), filtered, and evaporated to dryness, giving 3.80 g (80% yield from Boc-homophenylalaninal).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05976858
출처 데이터셋uspto-grants-1999_11
ORD IDord-acf3b734ba6c4d49893738d6d94827e3
출처 메모uspto-grants-1999_11