참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Methanesulfonic Acid | HCID 6395 | — |
| 반응물 | 1-Acetoxy-2-bromoethane | HCID 13564 | — |
| 반응물 | 2-(3-Bromo-4-methoxyphenyl)-2-methylpropionitrile | HCID 11368810 | — |
| 촉매 | Zinc | HCID 23994 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 4-(3-Bromo-4-methoxy-phenyl)-4-methyl-3-oxo-pentanoic acid ethyl ester | HCID 66834665 | 72% |
반응 단계
To the THF suspension of zinc (5.72 g, 2 eq.), methanesulfonic acid (25.6 μl, 0.01 eq.) was added, and then stirred at 80° C. for 10 min. Then, the THF solution of 2-(3-bromo-4-methoxy-phenyl)-2-methyl-propionitrile (10 g, 39.35 mmol) was added, followed by addition of bromoethyl acetate (11.07 ml, 1.6 eq.) over 1 hr. The mixture was further stirred for 30 min. To the reaction solution, 4 M hydrochloric acid was added, and stirred at room temperature overnight. After extraction with ethyl acetate, the organic layer was washed with brine and dried over sodium sulfate. The drying agent was removed by filtration and the residues obtained after concentration under reduced pressure were purified by silica gel column chromatography (ethyl acetate/hexane) to obtain the title compound (orange oily substance, 9.74 g, 72%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09440922B2 |
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| 출처 데이터셋 | uspto-grants-2016_09 |
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| ORD ID | ord-e3caf457cc424c3a82933351d7c7f175 |
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| 출처 메모 | uspto-grants-2016_09 |
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