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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Boron trifluoride etherate | HCID 8000 | — |
| 반응물 | Lithium phenylacetylide | HCID 3437284 | — |
| 반응물 | tert-Butyl 1-oxa-6-azaspiro(2.5)octane-6-carboxylate | HCID 22135564 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | tert-Butyl 4-hydroxy-4-(3-phenylprop-2-ynyl)piperidine-1-carboxylate | HCID 86627346 | 91.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08518916B2 |
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| 출처 데이터셋 | uspto-grants-2013_08 |
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| ORD ID | ord-aad17222f93344df9a3fc42be36177bf |
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| 출처 메모 | uspto-grants-2013_08 |
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