참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium bisulfate | HCID 516920 | — |
| 반응물 | 1,1-Dimethylethyl N-((1S)-2-(methoxymethylamino)-2-oxo-1-(phenylmethyl)ethyl)carbamate | HCID 11055945 | — |
| 반응물 | Aluminium lithium hydride | HCID 21226445 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | tert-butyl N-[(2S)-1-oxo-3-phenylpropan-2-yl]carbamate | HCID 6998013 | — |
반응 단계
A mechanically stirred suspension of lithium aluminum hydride (6.59 g, 0.165 mol) in ether (1 L) was cooled to -45° C. under nitrogen. A solution of the product from Step A (0.150 mol) in ether (150 mL) was added, maintaining the temperature below -35° C. When the addition was complete, the reaction was warmed to 5° C., then recooled to -45° C. A solution of potassium hydrogen sulfate (36.1 g, 0.265 mol) in water was slowly added, maintaining the temperature below -5° C. After quenching, the reaction was stirred at room temperature for 1 h. The mixture was filtered through Celite, the ether evaporated, and the remainder partitioned between ethyl acetate and 2% potassium hydrogen sulfate. After washing with saturated brine, drying over magnesium sulfate and solvent removal, the title compound was obtained.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05859012 |
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| 출처 데이터셋 | uspto-grants-1999_01 |
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| ORD ID | ord-9076447184b9488f8a35983007bd93a5 |
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| 출처 메모 | uspto-grants-1999_01 |
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