反応式
C(=O)/C=C/C1C=CC=CC=1.[OH:11][CH2:12][CH:13]([CH2:15][OH:16])[OH:14].C1(CCC[CH2:26][CH:27]([OH:30])[CH2:28][OH:29])C=CC=CC=1.C1(CCCCC(O)CO)CCCCC1>[Pd]>[CH2:12]([O:11][CH2:26][CH:27]([CH2:28][OH:29])[OH:30])[CH:13]([CH2:15][OH:16])[OH:14]参加物
反応条件
- 温度
- 200 °C
実験手順
Trans-Cinnamaldehyde (13.2 g, 12.6 ml, 0.1 mol) of, glycerol (92.09 g, 73.7 ml, 1 mol) and 10% Pd/C (0.66 g, 5 wt % relative to the aldehyde) are charged to a Parr reactor, purged three times with nitrogen, heated to 200° C. with stirring and reacted at 1000 psi of hydrogen for 20 h. GC analysis shows complete consumption of the aldehyde. The mixture is filtered, the product extracted with ether (50 ml×5), and the combined ether solution is dried with sodium sulfate. The solvent is evaporated and the residue chromatographed on silica gel using hexane-ethyl acetate from 5:1 to 1:1 to give 4.6 g of the monoether (95% purity). This product is approximately a 2:1 mixture of 3-(3-phenylpropyl)-1,2-propanediol and 3-(3-cyclohexylpropyl)-1,2-propanediol. The individual components of this mixture are separated by second column chromatography and characterized by 1H and 13C NMR.
後処理
- custompurged three times with nitrogen
- customreacted at 1000 psi of hydrogen for 20 h
- customconsumption of the aldehyde
- filtrationThe mixture is filtered
- extractionthe product extracted with ether (50 ml×5)
- dry with materialthe combined ether solution is dried with sodium sulfate
- customThe solvent is evaporated
- customthe residue chromatographed on silica gel
- customto give 4.6 g of the monoether (95% purity)
- customThe individual components of this mixture are separated by second column chromatography
出典と根拠
- ORDレコード
- ord-342992f44ebe4a15b292da19cb4b52ce
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08829229B2
関連ノート
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