참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethylene Glycol | HCID 174 | — |
| 반응물 | Nitrogen | HCID 947 | — |
| 반응물 | Trimethyl orthoformate | HCID 9005 | — |
| 반응물 | 1-(2-Bromo-1,3-thiazol-5-yl)ethan-1-one | HCID 57562813 | — |
| 용매 | Sodium Bicarbonate | HCID 516892 | — |
| 생성물 | 2-Bromo-5-(2-methyl-[1,3]dioxolan-2-yl)-thiazole | HCID 66820078 | — |
반응 단계
In a flame dried round-bottomed flask equipped with a magnetic stir bar and a condenser under inert atmosphere (N2), a solution of 1-(2-bromo-thiazol-5-yl)-ethanone (2.20 g, 10.68 mmol) in ethylene glycol (11.46 mL, 205.53 mmol) was treated with trimethylorthoformate (2.39 mL, 21.76 mmol) followed by LiBF4 (204 mg, 2.14 mmol). The reaction mixture was heated at 95° C. for 2 days. Sat. aq. NaHCO3 (50 mL) was added and the mixture was extracted with EA (50 mL). The org. extracts were washed with brine (2×50 mL), dried over MgSO4, filtered, and the solvent was removed under reduced pressure. Purification of the residue by FC (20:1 to 3:1 hept-EA) gave the title compound as a yellow oil. TLC:rf (1:1 hept-EA)=0.80. LC-MS-conditions 01: tR=0.84 min; [M+H]+=251.85.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08536209B2 |
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| 출처 데이터셋 | uspto-grants-2013_09 |
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| ORD ID | ord-47e77418a6244000a6972217938b3779 |
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| 출처 메모 | uspto-grants-2013_09 |
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