참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | (Iodomethyl)cyclopentane | HCID 2762531 | — |
| 반응물 | Methyl 2-(4-(methylsulfonyl)phenyl)acetate | HCID 16640928 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Methidathion | HCID 13709 | — |
| 생성물 | Methyl 3-cyclopentyl-2-(4-methylsulfonylphenyl)propionate | HCID 19261331 | — |
반응 단계
To a solution of diispropylamine (25 mmol, 3.6 mL) in 24 mL of THF and 7.5 mL of methidathion (DMTP) at −78° C. is added n-BuLi (25 mmol, 10 mL, 2.5 M in hexanes) and the mixture stirred for 15 min. 4-Methylsulfonylphenylacetic acid methyl ester (24 mmol, 5.47 g) in 24 mL of THF and 7.5 mL of DMTP is then added dropwise over 30 min and the reaction is stirred for 90 min further. Cyclopentylmethyliodide (28.9 mmol, 6.08 g) in 10 mL of THF is then added dropwise and the reaction is stirred for 1 h at −78° C. before allowing to warm to RT. After 12 h, the reaction is quenched with water, evaporated and then partitioned between ethyl acetate (EtOAc) and brine, and the organic solution is dried and evaporated to afford an oil. The crude material is chromatographed on silica (eluent: 5%→25% EtOAc in hexanes) to afford 3-cyclopentyl-2-(4-methanesulfonyl-phenyl)-propionic acid methyl ester.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07812167B2 |
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| 출처 데이터셋 | uspto-grants-2010_10 |
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| ORD ID | ord-d8ef0e9e40c04f8c93c5fde6d48cf5da |
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| 출처 메모 | uspto-grants-2010_10 |
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