(-)-2,2,2-Trifluoro-1-(9-anthryl)ethanol → (1R)-2-Methyl-1-methylthiocarbonyloxypropyl 2-methylpropanoate

HRID 558053ノート

反応式

HRID 558053 の反応式
[CH3:1][CH:2]([CH3:14])[C:3]([O:5][CH:6]([O:10][C:11]([CH3:13])=[S:12])[CH:7]([CH3:9])[CH3:8])=[O:4].FC(F)(F)[C@@H](C1C2C(C=C3C=1C=CC=C3)=CC=CC=2)O>OP([O-])(O)=O.OP([O-])([O-])=O.[Na+].[Na+].[Na+].[Cl-].[Cl-].[K+].[K+].CCOCC>[CH3:1][CH:2]([CH3:14])[C:3]([O:5][C@H:6]([O:10][C:11]([CH3:13])=[S:12])[CH:7]([CH3:8])[CH3:9])=[O:4]

参加物

5

反応物 2

HCID 7006444(-)-2,2,2-Trifluoro-1-(9-anthryl)ethanolHCID 866102712-Methyl-1-methylthiocarbonyloxypropyl 2-methylpropanoate

生成物 1

HCID 86633028(1R)-2-Methyl-1-methylthiocarbonyloxypropyl 2-methylpropanoate収率 24.3%

試薬・触媒・溶媒 2

HCID 3283Diethyl Ether溶媒HCID 24978514Phosphate Buffered Saline溶媒

実験手順

A mixture of 2-methyl-1-methylthiocarbonyloxypropyl 2-methylpropanoate (2b) (125 g) and lipase from Candida rugosa (Sigma-Aldrich) (12.5 g) in pH 7.2 phosphate buffered saline (1 L) was stirred at room temperature. The reaction was monitored by 1H-NMR using the chiral solvating agent (R)-(−)-2,2,2-trifluoro-1-(9-anthryl)ethanol. The reaction was stirred overnight. The reaction mixture was then diluted with ether, and the ether layer separated and filtered through a pad of CELITE® 545 to remove the enzyme. The ether layer was washed with aqueous sodium bicarbonate (NaHCO3) (5 times) and brine, and dried over anhydrous sodium sulfate (Na2SO4). After rotary evaporation to remove the solvent, 30.4 g of the title compound (4) was obtained. 1H-NMR using a chiral solvating agent confirmed the presence of a single isomer. The absolute configuration was determined by derivatization to a compound having known stereochemistry. 1H-NMR (CDCl3): δ 0.96 (d, J=6.8 Hz, 6H), 1.16 (d, J=6.8 Hz, 3H), 1.17 (d, J=6.8 Hz, 3H), 1.98-2.07 (m, 1H), 2.32 (s, 3H), 2.56 (septet, J=7.2 Hz, 1H), 6.67 (d, J=5.6 Hz, 1H) ppm.

後処理

  1. stirringThe reaction was stirred overnight
  2. customthe ether layer separated
  3. filtrationfiltered through a pad of CELITE® 545
  4. customto remove the enzyme
  5. washThe ether layer was washed with aqueous sodium bicarbonate (NaHCO3) (5 times) and brine
  6. dry with materialdried over anhydrous sodium sulfate (Na2SO4)
  7. customAfter rotary evaporation
  8. customto remove the solvent

出典と根拠

ORDレコード
ord-c00a6d597c4c4eb7adab089966690693
出典データセット
uspto-grants-2011_11
特許番号
US08062870B2

反応ノート

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