(-)-Mandelic acid → (s)-(+)-3-(4-Fluorobenzyl)piperidine mandelic acid salt
反応式
[F:1][C:2]1[CH:14]=[CH:13][C:5]([CH2:6][CH:7]2[CH2:12][CH2:11][CH2:10][NH:9][CH2:8]2)=[CH:4][CH:3]=1.[C:15]([OH:25])(=[O:24])[C@@H:16]([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)[OH:17]>C(#N)C>[C:15]([OH:25])(=[O:24])[CH:16]([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)[OH:17].[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:6][C@@H:7]2[CH2:12][CH2:11][CH2:10][NH:9][CH2:8]2)=[CH:13][CH:14]=1参加物
実験手順
The crude racemic 3-(4-fluorobenzyl)piperidine (2.0 g) was dissolved in 25 mL acetonitrile and heated to reflux. The solution was hazy. To this was added 1.56 g (1 equiv.) of (R)-(−) mandelic acid dissolved in 15 mL acetonitrile. Some initial precipitation occurred when the cooler solution was added but it did redissolve when refluxing resumed. The heat was turned off and small amounts of enantiomerically pure salt was added as the temperature dropped. At first the seed crystals dissolved, but when the temperature dropped to 75° C., they remained suspended in the stirred solution. After a few more degrees of cooling, crystal growth was obvious. Cooling was continued at the rate of 1 degree/min. At 50° C., the solution was filtered to recover 0.9 g of salt, which melted at 164° C. It was recrystallized from acetonitrile twice to give (S)-(+)-3-(4-fluorobenzyl)piperidine mandelic acid salt in 98% ee, and melting at 168-171° C.
後処理
- temperatureheated to reflux
- customSome initial precipitation
- additionwas added
- dissolutionit did redissolve when
- temperaturerefluxing
- additionsmall amounts of enantiomerically pure salt was added as the temperature
- additiondropped
- dissolutionAt first the seed crystals dissolved
- additionwhen the temperature dropped to 75° C.
- temperatureAfter a few more degrees of cooling
- temperatureCooling
- filtrationAt 50° C., the solution was filtered
- customto recover 0.9 g of salt, which melted at 164° C
- customIt was recrystallized from acetonitrile twice
出典と根拠
- ORDレコード
- ord-bb418970dadc4c989a7441cd9cca0ec4
- 出典データセット
- uspto-grants-2005_09
- 特許番号
- US06949546B2
反応ノート
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