참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Ethyl (chloroformyl)acetate | HCID 118030 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | Butanethioamide, 3-methyl- | HCID 3034257 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 5-Hydroxymethyl-2-(2-methylpropyl)thiazole | HCID 21085977 | — |
반응 단계
Isovalerothioamide (6.0 g, 51 mmol) and ethyl formylchloroacetate (Heterocycles 32 (4), 693-701, (1991), 5.0 g, 33 mmol) are dissolved in dry DMF (20 mL), and heated to 95 degrees C. for 4 hours. The reaction is subsequently cooled to 0 degrees C., and cold water (50 mL) is added. The mixture is basified to pH=8 with solid sodium bicarbonate, then extracted with ether (3×35 mL). The combined organic extracts are washed with water, then saline and dried over magnesium sulfate, filtered, and concentrated. The residue is purified by flash chromatography (ethyl acetate/hexanes 4-10% elution) to give the desired product. NMR (CDCl3, 300 MHz) δ 8.27, 4.45-4.30, 3.70-3.50, 3.00-2.80, 2.30-2.10, 1.40-1.20, and 1.10-0.90.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07727997B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-75f58f65667748a0a0f97a393217bc0e |
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| 출처 메모 | uspto-grants-2010_06 |
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