関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Diisopropyl Ether | HCID 7914 | — |
| 反応物 | Acetic Anhydride | HCID 7918 | — |
| 反応物 | 2-Bromo-1-(3-chlorophenyl)ethanol | HCID 9964694 | — |
| 生成物 | (R)-2-bromo-1-(3-chlorophenyl)ethanol | HCID 11075396 | — |
| 生成物 | (S)-2-bromo-1-(3-chlorophenyl)ethyl acetate | HCID 11747860 | — |
反応手順
To 100 mg (0.4 mmol) of 2-bromo-1-(3-chlorophenyl)ethanol were added 30 mg of Lipase QL (available from Meito Sangyo Co., Ltd.) and 40 mg (0.4 mmol) of acetic anhydride. Diisopropyl ether was added to the mixture to make the total volume to 1 ml. The reaction mixture was then allowed to undergo reaction at a temperature of 35° C. for 72 hours. After the termination of the reaction, the enzyme was removed by filtration. The resulting filtrate was then concentrated under reduced pressure. The concentrated solution was analyzed by 1H-NMR. As a result, it was found that (R)-2-bromo-1-(3-chlorophenyl) ethanol and (S)-2-bromo-1-(3-chlorophenyl)ethyl acetate had been produced in a proportion of 2:3. The concentrated solution was then separated by a thin layer silica gel chromatography. As a result, (R)-2-bromo-1-(3-chlorophenyl)ethanol ([α]D20 =-25.6°, C=1.05) and (S)-2-bromo-1-(3-chlorophenyl)ethyl acetate ([α]D20 =+40.4°, C=0.60) were obtained. The optical purity of (R)-2-bromo-1-(3-chlorophenyl)ethanol thus obtained was analyzed by Chiral HPLC. The results were 100% ee.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US05841001 |
|---|
| 出典データセット | uspto-grants-1998_11 |
|---|
| ORD ID | ord-f640bfcaaa3b458781a31bff37f1c3b1 |
|---|
| 出典メモ | uspto-grants-1998_11 |
|---|