참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | p-Bromobenzyl chloride | HCID 68528 | — |
| 반응물 | Thiomorpholine 1,1-dioxide | HCID 6484228 | — |
| 용매 | Acetone | HCID 180 | — |
| 생성물 | 4-(4-Bromo-benzyl)-thiomorpholine 1,1-dioxide | HCID 52325468 | — |
반응 단계
To a well stirred suspension of thiomorpholine 1,1-dioxide (0.36 g, 2.7 mmol) and potassium carbonate (0.37 g, 2.7 mmol) in acetone (5 mL) was added 1-bromo-4-chloromethyl-benzene (0.50 g, 2.4 mmol). The mixture was stirred for 48 hours at room temperature. The mixture was filtered and the volatiles were evaporated. The residue was suspended in ether (100 mL), filtered and evaporated to a solid. The material was purified via chromatography utilizing an ISCO automated purification apparatus (24 g silica gel column 10%→100% ethyl acetate in hexane). 4-(4-Bromo-benzyl)-thiomorpholine 1,1-dioxide was isolated as a white solid (0.72 g, 97%). 1H NMR (400 MHz, CDCl3, δ, ppm): 7.47 (d, J=7.6 Hz, 2H), 7.19 (d, J=7.7 Hz, 2H), 3.60 (s, 2H), 3.08-2.94 (m, 8H). MS=304, 306 (MH)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08633173B2 |
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| 출처 데이터셋 | uspto-grants-2014_01 |
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| ORD ID | ord-d31aa3f94bd74546ac9e0316d120c040 |
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| 출처 메모 | uspto-grants-2014_01 |
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