Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 518178생성일: 2026년 10월 26일
Methyl Acrylate → (E)-3-{1'-benzyl-4-hydroxy-spiro[chromane-2,4'-piperidine]-6-yl}-acrylic acid methyl ester
https://huagongshe.com/reaction/518178
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Methyl Acrylate | HCID 7294 | — |
| 반응물 | (E)-3-{1'-tert-butoxycarbonyl-4-oxo-spiro[chromane-2,4'-piperidine]-6-yl}-acrylic acid methyl ester | HCID 52952087 | — |
| 반응물 | 1'-Benzyl-6-bromo-4-hydroxy-spiro[chromane-2,4'-piperidine] | HCID 52952196 | — |
| 생성물 | (E)-3-{1'-benzyl-4-hydroxy-spiro[chromane-2,4'-piperidine]-6-yl}-acrylic acid methyl ester | HCID 67286920 | — |
반응 단계
1′-Benzyl-6-bromo-4-hydroxy-spiro[chromane-2,4′-piperidine] (3.0 g, 7.7 mmol, Intermediate 3) was treated with methyl acrylate according to the procedure for preparation of Intermediate 1, Step B, giving (E)-3-{1′-benzyl-4-hydroxy-spiro[chromane-2,4′-piperidine]-6-yl}-acrylic acid methyl ester (3.1 g). The crude intermediate was dissolved in THF (20 ml) under N2 and p-TsOH (0.15 g, 0.79 mmol) was added. The mixture was heated to reflux. After 16 h, the mixture was poured into water and a 10% NaOH solution was added until reaching a neutral pH value. The solution was extracted with DCM, dried over Na2SO4, filtered and evaporated under vacuum. The crude mixture was purified by column chromatography using DCM/MeOH (90/10) and then hexane/AcOEt (70/30) as eluent to give (E)-3-{1′-benzyl-spiro[chromene-2,4′-piperidine]-6-yl}-acrylic acid methyl ester (150 mg).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09115148B2 |
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| 출처 데이터셋 | uspto-grants-2015_08 |
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| ORD ID | ord-68d171e3cd4045469f53e0f0e6e695f1 |
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| 출처 메모 | uspto-grants-2015_08 |
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