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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 931342생성일: 2026년 10월 23일

Hydrochloric Acid → Ethyl 2-amino-3-oxo-3-(tetrahydrofuran-3-yl)propanoate, hydrochloride salt

https://huagongshe.com/ko/reaction/931342

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물Tetrahydrofuran-3-carbonyl chlorideHCID 14020412—
반응물HCID 178472686HCID 178472686—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 2-amino-3-oxo-3-(tetrahydrofuran-3-yl)propanoate, hydrochloride saltHCID 131732346—

반응 단계

Lithium bis(trimethysilyl)amide (1 M solution in tetrahydrofuran, 288 mL, 0.288 mol) was added drop-wise to a solution of ethyl (2E)-[(diphenylmethyl)imino]ethanoate (70 g, 0.26 mol) in tetrahydrofuran (1 L) at −70° C. The reaction mixture was stirred for 30 minutes, and the resulting suspension was transferred via cannula into a solution of tetrahydrofuran-3-carbonyl chloride (35.7 g, 0.26 mol) in tetrahydrofuran (200 mL) at −70° C. The reaction mixture was stirred at room temperature for 2 hours, at which time aqueous hydrochloric acid (2 M, 260 mL) was added. After the reaction mixture had stirred for 15 minutes, the tetrahydrofuran was removed in vacuo, and the aqueous residue was washed with ethyl acetate (4×200 mL). The aqueous layer was freeze-dried, affording the product as a light yellow solid. Yield: 40 g, 0.20 mol, 77%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09296761B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-ed521298f98e4cc5b0e037e5c4519664
출처 메모uspto-grants-2016_03