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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 731552생성일: 2026년 10월 24일

Hydrochloric Acid → (R)-Benzyl (5-oxotetrahydrofuran-3-yl)carbamate

https://huagongshe.com/ko/reaction/731552

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물EthanolHCID 702—
반응물Sodium borohydrideHCID 4311764—
반응물(R)-Benzyl (2,5-dioxotetrahydrofuran-3-yl)carbamateHCID 12416472—
용매TetrahydrofuranHCID 8028—
용매Sodium chloride; waterHCID 57417360—
생성물(R)-Benzyl (5-oxotetrahydrofuran-3-yl)carbamateHCID 69792451.1%

반응 조건

온도0 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07585858B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-8addecd12fac44649e93f644e206c2b7
출처 메모uspto-grants-2009_09