참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrogen Peroxide | HCID 784 | — |
| 반응물 | Triethylborane | HCID 7357 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | 1-Iodopropane | HCID 33643 | — |
| 반응물 | 4,5,6,7-Tetrahydro-4-oxothionaphthene | HCID 83418 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 5-propyl-6,7-dihydro-1-benzothiophen-4(5H)-one | HCID 22147491 | 80% |
반응 단계
To a solution of KH (30%, 11.44 g) in tetrahydrofuran (160 ml) under N2 was added dropwise 6,7-dihydro-1-benzothiophen-4(5H)-one (8 g) in tetrahydrofuran (40 ml). After 30 min, a triethyl borane (97 ml, 1 M THF) solution was added dropwise over 5 min. After 10 min, iodopropane was and the reaction stirred for 16 h. The reaction mixture was cooled to 0° C. and 1 N NaOH (250 ml) and hydrogen peroxide (12 ml, 30%) was added. The reaction mixture stirred for 1 h and was extracted with 400 ml ethyl acetate. The organic layer was washed with saturated sodium thiosulfate, dried MgSO4, filtered and concentrated. MPLC chromatography on a biotage 40 L with 4% ethyl acetate/heptane provided the title compound as an oil (8.21 g, 80%): 1H NMR (300 MHz, CDCl3) δ) 7.40, 7.07, 3.15-3.01, 2.47, 2.32, 2.07-1.88, 1.53-1.30, 1.27, 0.99-0.88; HRMS (FAB) calcd for C11H14OS+H 195.0844, found 195.0835.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06992087B2 |
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| 출처 데이터셋 | uspto-grants-2006_01 |
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| ORD ID | ord-525ae72c613f43ab87f0b367dd87f09b |
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| 출처 메모 | uspto-grants-2006_01 |
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