참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Lawesson's reagent | HCID 87949 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | Oxane-4-carboxamide | HCID 13197203 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Oxane-4-carbothioamide | HCID 13197204 | 87.5% |
반응 단계
A solution of tetrahydro-2H-pyran-4-carboxamide (9.47 g, 73.3 mmol) and Lawesson's reagent (14.83 g, 36.7 mmol) in THF (98 mL) was heated to reflux for 6 h. The reaction was cooled to rt, poured into saturated aqueous NaHCO3 (200 mL) and extracted with diethyl ether (4×100 mL). The combined organic extracts were dried over Na2SO4, filtered, and concentrated. The residual solid was triturated with 1:1 EtOAc:hexanes (100 mL) and filtered to collect the solid. The filtrate was concentrated and re-subjected to trituration and filtration using the same conditions. The combined solids were dried under vacuum to afford tetrahydro-2H-pyran-4-carbothioamide (4.91 g, 32.1 mmol, 43.8% yield) as a white solid. 1H NMR (400 MHz, CDCl3) δ ppm 7.49 (br. s., 1H), 6.84 (br. s., 1H), 3.94-4.32 (m, 2H), 3.31-3.62 (m, 2H), 2.52-3.03 (m, 1H), 1.81-1.93 (m, 4H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08642759B2 |
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| 출처 데이터셋 | uspto-grants-2014_02 |
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| ORD ID | ord-7da2d16f7e3c417fa2892031a82a7d54 |
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| 출처 메모 | uspto-grants-2014_02 |
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