참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 3-[3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-phenyl]-acrylic Acid Methyl Ester | HCID 67396155 | — |
| 반응물 | HCID 178449909 | HCID 178449909 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | HCID 136413210 | HCID 136413210 | — |
반응 단계
A solution of N-hydroxy-butyramidine (0.24 g, 2.34 mmol) in tetrahydrofuran (5 mL) was added slowly into the suspension of 60% sodium hydride (0.14 g, 3.5 mmol) in dry tetrahydrofuran (5 mL) under nitrogen atmosphere at 0° C. to 10° C. The mixture was stirred for 30 min at room temperature. 3-[3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-phenyl]-acrylic acid methyl ester (compound of Example 1, Step 1; 0.5 g, 1.18 mmol) in dry tetrahydrofuran (5 mL) was added into the reaction mixture and heated at 60° C. for 8 h. The reaction mixture was cooled at 0° C. and quenched with methanol (2 mL) to destroy excess sodium hydride. The reaction mixture was extracted with ethyl acetate (2×10 mL) and the combined organic layers were washed with water (2×10 mL) followed by brine (10 mL). The organic phase obtained was dried over anhydrous sodium sulphate and concentrated to dryness. The crude product obtained was purified by column chromatography (silica gel, chloroform-methanol) to afford the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08629277B2 |
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| 출처 데이터셋 | uspto-grants-2014_01 |
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| ORD ID | ord-4c664d48321d4babab4ca34308e1347e |
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| 출처 메모 | uspto-grants-2014_01 |
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