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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 324766생성일: 2026년 10월 26일

Hydrochloric Acid → 3-Phenylpropyl 4-(2-(1-piperidinyl)ethoxy)acetoacetate

https://huagongshe.com/reaction/324766

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물N-PiperidinoethanolHCID 18232—
반응물Sodium hydrideHCID 24758—
반응물3-Phenylpropyl 4-chloroacetoacetateHCID 22005546—
용매TetrahydrofuranHCID 8028—
생성물3-Phenylpropyl 4-(2-(1-piperidinyl)ethoxy)acetoacetateHCID 2200551267.1%

반응 단계

2-(1-Piperidinyl)ethanol (15 mL, 113 mmol) in THF (50 mL) was added dropwise to a suspension of sodium hydride (7 g, 175 mmol) in THF (200 mL) at 0° C. The mixture was then stirred for 1 h at room temperature, cooled to 0° C., 3-phenylpropyl 4-chloroacetoacetate (22 mL, 103 mmol) in THF (50 mL) was added dropwise and the reaction mixture was then stirred for 18 h whilst warming to room temperature. 1N Hydrochloric acid was added until the mixture was acidic and the aqueous layer was then separated. The organic layer was extracted twice more with 1N hydrochloric acid. The combined acid layers were made basic to pH 8 with sodium hydrogen carbonate and extracted with chloroform. The combined extracts were washed with brine, dried and evaporated to give the title compound (24 g) as an oil. Electrospray MS m/z 348 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06218538B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-a9f7ca5fb7cf4d46a7a423dcaa90353b
출처 메모uspto-grants-2001_04