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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 716296생성일: 2026년 10월 24일

Acetone → Ethyl 2-((propan-2-yl)amino)acetate

https://huagongshe.com/ko/reaction/716296

반응식

참여 물질

역할이름HCID투입량
반응물AcetoneHCID 180—
반응물Sodium HydroxideHCID 14798—
반응물Glycine ethyl ester, hydrochlorideHCID 2723640—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물Ethyl 2-((propan-2-yl)amino)acetateHCID 35162585%

반응 단계

To a suspension of ethyl 2-aminoacetate hydrochloride (20 g, 143.28 mmol) in THF (400 mL) was added glacial acetic acid (20 mL) followed by acetone (11.59 mL, 151.62 mmol). The reaction was stirred 30 min at room temperature. Sodium triacetoxyborohydride (60.73 g, 286.56 mmol) was added over the course of one hour. The reaction was poured slowly into a vigorously stirred biphasic mixture of water (300 mL) and ethyl acetate (800 mL). The aqueous layer was adjusted to pH 13 using a solution of 50% (weight) NaOH. The mixture was stirred 30 min and poured into a separatory funnel. The organic layer was collected and the aqueous layer was back extracted with ethyl acetate (3×200 mL). The organic layers were combined, washed with brine (300 mL), dried with sodium sulfate, and concentrated to yield the title compound (17.6 g, 85%) as a translucent oil which was used in the next step without further purification. [M+H] calc'd for C7H15NO2, 146. found, 146.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09187497B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-8aa297fada614315ac17fdf39e9d0a71
출처 메모uspto-grants-2015_11