참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | tert-Butyl acetate | HCID 10908 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Perchloric Acid | HCID 24247 | — |
| 반응물 | L-Glutamic Acid | HCID 33032 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | L-Glutamic acid di-tert-butyl ester | HCID 208637 | 41% |
반응 단계
Acetic acid 1,1-dimethylethyl ester (1742 g; 2 L; 15 mol) (commercial product), 70% aq. perchloric acid (51 mL; 0.59 mol) and L-glutamic acid (78.8 g; 0.54 mol) (commercial product) were stirred at 25° C. over 5 days. After addition of a solution of K2CO3 (41.46 g, 0.3 mol) in H2O (140 mL) to the reaction mixture, the organic phase was separated, washed with water (2×500 mL), dried (NaSO4) and concentrated to dryness. The residue (27.2 g) was dissolved in Et2O (200 mL) and extracted with 1N HCl (2×70 mL), the combined aqueous phase was washed with Et2O (40 mL) and collected with the aqueous phases previously obtained from the first neutralization and successive washings. Addition of 10 N NaOH up to pH 8.8 led to an emulsion which was extracted with Et2O (2×600 mL). The combined organic phases were washed with H2O (250 mL), dried and evaporated to give the desired compound (57.7 g; 0.22 mol). Yield 41%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06403055B1 |
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| 출처 데이터셋 | uspto-grants-2002_06 |
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| ORD ID | ord-7255903b82b040459b8d14d1553a6454 |
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| 출처 메모 | uspto-grants-2002_06 |
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