참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Malonic Acid | HCID 867 | — |
| 반응물 | Piperidine | HCID 8082 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | 5-(4-fluorophenyl)-1-methyl-1H-pyrazole-4-carbaldehyde | HCID 23157484 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Diglyme | HCID 8150 | — |
| 생성물 | (2E)-3-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]acrylic acid | HCID 69208981 | 90% |
반응 단계
To a mixture of 5-(4-fluorophenyl)-1-methyl-1H-pyrazole-4-carbaldehyde (3.00 g), malonic acid (1.99 g) and bis(2-methoxyethyl) ether (9 mL) was added dropwise piperidine (1.89 mL) over about 10 min. The mixture was stirred at 90-95° C. for 1 hr. and further at 105-110° C. for 4 hrs. After cooling to 25° C., toluene (12 mL) and 1N aqueous sodium hydroxide solution (15 mL) were added and the mixture was stirred. The aqueous layer was separated and the organic layer was extracted with 1N aqueous sodium hydroxide solution (6 mL). The aqueous layers were combined and washed with toluene. The layers were adjusted to pH 3.5-4.0 with 2N hydrochloric acid at 20-30° C. and water (9 mL) was added dropwise. After stirring at 25° C. for 1 hr., the precipitated crystals were collected by filtration and washed with 20% ethanol to give (2E)-3-[5-(4-fluorophenyl)-1-methyl-1H-pyrazol-4-yl]acrylic acid (3.24 g, yield 90%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07423159B2 |
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| 출처 데이터셋 | uspto-grants-2008_09 |
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| ORD ID | ord-db6aa61893614edf9ca87b9570f1139c |
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| 출처 메모 | uspto-grants-2008_09 |
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