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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1434523생성일: 2026년 10월 27일

Methyl iodide → Benzyl ((3R,4R)-4-methyl-5-oxotetrahydrofuran-3-yl)carbamate

https://huagongshe.com/reaction/1434523

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물DiisopropylamineHCID 7912—
반응물Ammonium ChlorideHCID 25517—
반응물(R)-Benzyl (5-oxotetrahydrofuran-3-yl)carbamateHCID 697924—
반응물ButyllithiumHCID 178418339—
촉매ICE protocol 1HCID 56841950—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물Benzyl ((3R,4R)-4-methyl-5-oxotetrahydrofuran-3-yl)carbamateHCID 13108321—

반응 조건

온도0 °C

반응 단계

272 μl (1.9 mmol) diisopropylamine are placed in 3 ml THF and while cooling with ice 1.2 ml (1.9 mmol) of an n-butyllithium solution in hexane (1.6M) are added. The mixture is stirred for 10 minutes at 0° C., then cooled to −78° C. and a solution of 200 mg (0.85 mmol) benzyl (R)-(5-oxo-tetrahydrofuran-3-yl)-carbamate in 1 ml THF is added dropwise. The mixture is stirred for one hour at −78° C. Then 210 μl (3.3 mmol) methyl iodide are added dropwise, and the mixture is heated to −60° C. within one hour. Then 0.5 ml sat. ammonium chloride solution is added and the mixture is heated to ambient temperature. Water is added and the mixture is extracted three times with ethyl acetate. The combined organic phases are dried over sodium sulphate and evaporated to dryness. The residue is taken up in DMF, acidified with TFA and purified by reversed-phase chromatography.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07615549B2
출처 데이터셋uspto-grants-2009_11
ORD IDord-5b312c38ffbe4103ae25f7061656ab9e
출처 메모uspto-grants-2009_11