참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Trimethyl orthoformate | HCID 9005 | — |
| 반응물 | Trimethylolmethane | HCID 78432 | — |
| 반응물 | 1,3-Difluoroacetone | HCID 228397 | — |
| 반응물 | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| 용매 | Triethylamine | HCID 8471 | — |
| 생성물 | (2,2-Bis(fluoromethyl)-1,3-dioxan-5-yl)methanol | HCID 59792580 | 43.4% |
반응 단계
A mixture of 2-(hydroxymethyl)-1,3-propanediol (2.2 g, 20.7 mmol), 1,3-difluoroacetone (3.89 g, 41.4 mmol), trimethyl orthoformate (3.44 ml, 20.7 mmol), and p-toluenesulfonic acid monohydrate (356 mg, 2.07 mmol) was stirred at 60° C. for 10 hours. After completion of the reaction, triethylamine (577 μl) was added to the reaction mixture, which was then concentrated. The residue was purified by silica gel column chromatography (elution solvent: heptane/ethyl acetate) to obtain the title compound (1.6 g, yield: 43.4%) as a light yellow oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07425634B2 |
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| 출처 데이터셋 | uspto-grants-2008_09 |
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| ORD ID | ord-643f1dd86f91404aa5f5e314bc0f49bb |
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| 출처 메모 | uspto-grants-2008_09 |
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