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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16347생성일: 2026년 10월 24일

Ammonium Chloride → tert-butyl {(S)-1-benzyloxymethyl-2-[2-oxo-2-(3,4,5-trifluorophenyl)ethoxy]ethyl}carbamate

https://huagongshe.com/ko/reaction/16347

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물1-Bromo-3,4,5-trifluorobenzeneHCID 611409—
반응물MagnesiumHCID 5462224—
반응물tert-butyl(S)-3-benzyloxymethyl-5-oxomorpholine-4-carboxylateHCID 67373012—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물tert-butyl {(S)-1-benzyloxymethyl-2-[2-oxo-2-(3,4,5-trifluorophenyl)ethoxy]ethyl}carbamateHCID 67373700—

반응 조건

온도40 °C

반응 단계

1-Bromo-3,4,5-trifluorobenzene (446 μL) was dropwise added to a diethylether suspension (5 mL) of magnesium (249 mg) over 10 min at 40° C. The resulting reaction solution was stirred at 40° C. for 1 hr and then dropwise added to a tetrahydrofuran solution (30 mL) of (S)-3-benzyloxymethyl-5-oxomorpholine-4-carboxylic acid tert-butyl ester (1.1 g) over 10 min at −40° C. The resulting reaction solution was stirred at −40° C. for 1 hr, and a saturated ammonium chloride aqueous solution was gradually added dropwise thereto at −40° C. The resulting reaction solution was warmed up to room temperature, and then ethyl acetate was added thereto. The organic layer was separated, washed with saturated saline, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (heptane-ethyl acetate system) to give 952 mg of the title compound. The physical property values of this compound were as follows:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737141B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-1cfeb729204c45378d4035f81c16e13b
출처 메모uspto-grants-2010_06