참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Cinchonidine | HCID 101744 | — |
| 반응물 | Cyclohexyl-hydroxy-thiophen-2-yl-acetic acid | HCID 13063448 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | Cinchonidine | HCID 101744 | — |
| 생성물 | (S)-Cyclohexyl-hydroxy-thiophen-2-yl-acetic acid | HCID 67538134 | — |
반응 단계
L-cinchonidine (30.2 g, 0.103 mol) is added to crude cyclohexyl-hydroxy-thiophen-2-yl-acetic acid (49.3 g, 103 mol assuming 50% purity of crude) followed by toluene (2.2 litres) and the mixture is heated to reflux for 70 minutes. The resulting solution is allowed to cool slowly and at 65° C., the solution is seeded. After further cooling to 40° C., the solution is placed in the fridge overnight. The resulting solid is filtered, washed with toluene and dried in vacuo. The recrystallisation process from toluene is repeated for a second time with seeding occurring at 85° C. to afford the titled compound as a salt of L-cinchonidine in 98% enantiomeric excess. The salt is added to a stirred mixture of 1M HCl (40 ml) and diethyl ether (500 ml) and stirring continues until a solution forms. The organic portion is separated, washed with brine (400 ml), dried over MgSO4 and concentrated in vacuo to give the titled compound in 98% enantiomeric excess.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08084463B2 |
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| 출처 데이터셋 | uspto-grants-2011_12 |
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| ORD ID | ord-6330bc72192743148861809a836e03d9 |
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| 출처 메모 | uspto-grants-2011_12 |
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