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Ethyl behenate → 1-Phenylethanol, (R)-

HRID 1939749
ノート
印刷プレビュー

反応式

HRID 1939749 の反応式
C([O:24][C@@H:25]([C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1)[CH3:26])(=O)CCCCCCCCCCCCCCCCCCCCC.C(OCC)(=O)CCCCCCCCCCCCCCCCCCCCC>CC(C)=O>[C:27]1([C@H:25]([OH:24])[CH3:26])[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 22199Ethyl behenateHCID 54028439HCID 54028439、化合物

生成物 1

HCID 6375161-Phenylethanol, (R)-収率 88%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

反応条件

温度
5 °C

実験手順

Interesterification was carried out by using 1 g of Lipase QL, 40 g of (R,S)-1-phenylethanol, and 60 g of ethyl behenate under the same conditions as in Example 6 at 95° C. for a period of 20 hours. The water content of the reaction system was 0.03% by weight, and 95% of the lipase particles had a particle size of 20 to 40 μm. Gas chromatography of the reaction mixture revealed that 47 mol % of (R,S)-1-phenylethanol had been converted to 1-phenylethyl behenate. The reaction mixture was treated in the same manner as in Example 6 and subjected to simple distillation at 85° C. and 5 mmHg to give (S)-(-)-1-phenylethanol (yield: 97%; chemical purity: 99.9%; optical purity: 88.9% ee). On the other hand, the residue, i.e., a mixture of (R)-(+)-1-phenylethyl behenate and unreacted ethyl behenate was alkali-hydrolyzed in the same manner as in Example 1, and 1000 ml of acetone was added to the reaction mixture, followed by cooling to 5° C. The precipitated behenic acid was removed by filtration to obtain (R)-(+)-1-phenylethanol (yield: 88%; chemical purity: 99.9%; optical purity: 98.5% ee).

後処理

  1. additionwas added to the reaction mixture
  2. customThe precipitated behenic acid was removed by filtration

出典と根拠

ORDレコード
ord-e2c580acacfc4be2971ad3a5707ce998
出典データセット
uspto-grants-1997_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05696299

反応ノート

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