참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl (4-chlorophenyl)acetate | HCID 84177 | — |
| 반응물 | Lithium diisopropylamide | HCID 2724682 | — |
| 반응물 | (Iodomethyl)cyclopentane | HCID 2762531 | — |
| 용매 | Hexamethylphosphoramide | HCID 12679 | — |
| 용매 | tetrahydrofuran HMPA | HCID 86583969 | — |
| 생성물 | HCID 46221154 | HCID 46221154 | 90.9% |
반응 단계
A solution of freshly prepared lithium diisopropylamide (23.0 mL of 0.31M stock solution, 7.13 mmol) cooled to −78° C. was treated with (4-chloro-phenyl)-acetic acid ethyl ester (1.28 g, 6.48 mmol) in tetrahydrofuran/hexamethylphosphoramide (16.1 mL, 3:1). The resulting solution was stirred at −78° C. for 45 min. At this time, the reaction was treated with a solution of iodomethylcyclopentane (1.50 mg, 7.13 mmol) in hexamethylphosphoramide (1 mL). The reaction-mixture was stirred at −78° C. for 4 h. The reaction was warmed to 25° C. and stirred at 25° C. for 16 h. The reaction mixture was then quenched by the dropwise addition of a saturated aqueous ammonium chloride solution (20 mL). This mixture was poured into water (100 mL) and extracted with ethyl acetate (3×50 mL). The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 75/25 hexanes/ethyl acetate) afforded 2-(4-chloro-phenyl)-3-cyclopentyl-propionic acid ethyl ester (1.65 g, 90.9%) as a yellow oil: EI-HRMS m/e calcd for C16H21Cl2O2 (M+) 280.1230, found 280.1227.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06610846B1 |
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| 출처 데이터셋 | uspto-grants-2003_08 |
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| ORD ID | ord-6c8c483c00954e319776c71002fb2ab0 |
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| 출처 메모 | uspto-grants-2003_08 |
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