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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1896010생성일: 2026년 10월 26일

Boron trifluoride etherate → tert-Butyl 4-hydroxy-4-(3-phenylprop-2-ynyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1896010

반응식

참여 물질

역할이름HCID투입량
반응물Boron trifluoride etherateHCID 8000—
반응물Lithium phenylacetylideHCID 3437284—
반응물tert-Butyl 1-oxa-6-azaspiro(2.5)octane-6-carboxylateHCID 22135564—
용매TetrahydrofuranHCID 8028—
생성물tert-Butyl 4-hydroxy-4-(3-phenylprop-2-ynyl)piperidine-1-carboxylateHCID 8662734691.9%

반응 조건

온도-75 °C

반응 단계

Boron trifluoride diethyl etherate (0.131 mL, 1.03 mmol) followed by lithium phenylacetylide (1M in THF, 1.03 mL, 1.03 mmol) was dropped into a solution of Compound 256a (200 mg, 0.938 mmol) in THF (5 mL) stirred at −75° C. under nitrogen atmosphere. Stirring and cooling were kept on for 2 h and after overnight stirring at r.t., the reaction mixture was quenched with water and EtOAc. The combined extracts were washed, dried over Na2SO4 and evaporated to dryness. The residue was purified by flash chromatography (EtOAc—Petroleum Ether 85:15) affording the title product (272 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08518916B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-aad17222f93344df9a3fc42be36177bf
출처 메모uspto-grants-2013_08