참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Ethanol | HCID 702 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 반응물 | (R)-Benzyl (2,5-dioxotetrahydrofuran-3-yl)carbamate | HCID 12416472 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Sodium chloride; water | HCID 57417360 | — |
| 생성물 | (R)-Benzyl (5-oxotetrahydrofuran-3-yl)carbamate | HCID 697924 | 51.1% |
반응 단계
A suspension of NaBH4 (2.71 g, 71.5 mmol) in THF (50 mL) was cooled to 0° C., treated dropwise with a solution of EXAMPLE 21A (16.21 g, 65.0 mmol) in THF (50 mL), allowed to warm to room temperature, and stirred for 2 hours. The resulting mixture was treated with concentrated HCl (13.1 mL) and ethanol (13.1 mL), heated to reflux for 12 hours, allowed to cool to room temperature, poured into brine (100 mL) and the layers were separated. The aqueous phase was extracted with ethyl acetate and the combined organic layers were washed with water and brine, dried (MgSO4), filtered, and concentrated. The concentrate was triturated with diethyl ether (50 mL) for 2 hours, cooled overnight, and the solid collected by filtration to provide the desired product (7.81 g, 51%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07585858B2 |
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| 출처 데이터셋 | uspto-grants-2009_09 |
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| ORD ID | ord-8addecd12fac44649e93f644e206c2b7 |
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| 출처 메모 | uspto-grants-2009_09 |
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