Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 539354생성일: 2026년 10월 27일
Ethyl Acetate → N-(6-Bromo-5',6'-dihydro-4'H-spiro[chromene-2,3'-pyran]-4(3H)-ylidene)-2-methylpropane-2-sulfinamide
https://huagongshe.com/reaction/539354
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | Tert-Butanesulfinamide | HCID 3382465 | — |
| 반응물 | 6-Bromo-2',4',5',6'-tetrahydrospiro[chroman-2,3'-pyran]-4-one | HCID 58423823 | — |
| 촉매 | Titanium tetraethoxide | HCID 76524 | — |
| 용매 | HCID 178479889 | HCID 178479889 | — |
| 생성물 | N-(6-Bromo-5',6'-dihydro-4'H-spiro[chromene-2,3'-pyran]-4(3H)-ylidene)-2-methylpropane-2-sulfinamide | HCID 67979337 | 97% |
반응 단계
6-Bromo-5′,6′-dihydro-4′H-spiro[chromene-2,3′-pyran]-4(3H)-one (Intermediate 26, 2.007 g, 6.75 mmol), 2-methylpropane-2-sulfinamide (1.228 g, 10.13 mmol) and titanium ethoxide (2.78 mL, 13.51 mmol) were dissolved in methyl THF (16 mL) and heated to reflux for 19 h. The reaction was left to cool down to r.t. when EtOAc (80 mL) and NaHCO3 (sat., 5 mL) were added under stirring. The mixture was let standing for 1 h. The organic phase was collected by filtration, dried over MgSO4 and concentrated. The crude product was purified by flash chromatography using a gradient of 0-50% EtOAc in heptane. The desired fractions were evaporated to give the title compound as a mixture of diastereomers in a ratio 1:1 as determined by NMR (2.63 g, 97% yield): 1H NMR (500 MHz, CDCl3) δ ppm 1.34 (s, 9H), 1.50-1.57 (m, 0.5H), 1.60-1.68 (m, 1H), 1.73 (m, 0.5H) 1.87-2.09 (m, 2H), 2.99 (d, 0.5H), 3.26 (d, 0.5H), 3.33 (d, 0.5H), 3.45-3.61 (m, 2H), 3.64 (d, 0.5H), 3.77-3.93 (m, 2H), 6.88-6.93 (m, 1H), 7.48 (dd, 1H), 7.98 (dd, 1H); MS (ES+) m/z 401.9 [M+H]+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08865911B2 |
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| 출처 데이터셋 | uspto-grants-2014_10 |
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| ORD ID | ord-9e093ea93e9c489a96d5ca3e47b79ab5 |
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| 출처 메모 | uspto-grants-2014_10 |
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