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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1025321생성일: 2026년 10월 24일

Benzoxazole → tert-butyl (2S)-1-(benzo[d]oxazol-2-yl)-1-hydroxybutan-2-ylcarbamate

https://huagongshe.com/ko/reaction/1025321

반응식

참여 물질

역할이름HCID투입량
반응물BenzoxazoleHCID 9228—
반응물Ammonium ChlorideHCID 25517—
반응물tert-butyl N-((2S)-1-oxobutan-2-yl)carbamateHCID 10241556—
반응물HCID 178418918HCID 178418918—
용매TetrahydrofuranHCID 8028—
생성물tert-butyl (2S)-1-(benzo[d]oxazol-2-yl)-1-hydroxybutan-2-ylcarbamateHCID 11522383—

반응 조건

온도-5 °C

반응 단계

Under an atmosphere of argon, benzo[d]oxazole (5 g, 42.0 mmol, Eq: 1.00) was combined with THF (100 ml) to give a light yellow solution. At −5° C. isopropylmagnesium chloride 2M in THF (21.0 ml, 42.0 mmol, Eq: 1.00) was added dropwise. The reaction was stirred for 1.5 h at −5° C. Then (S)-tert-butyl 1-oxobutan-2-ylcarbamate (4.72 g, 25.2 mmol, Eq: 0.6) diluted in 20 ml THF was added. The reaction was stirred overnight at RT. Satd. ammoniumchloride solution (6 ml) was added to the reaction. The THF was evaporated under vacuum. The reaction mixture was poured into 50 ml H2O and extracted with ethyl acetate (2×100 ml). The crude material was purified by flash chromatography (silica gel, 20 g, 0% to 40% ethyl acetate in heptane). The title compound was obtained as a brown gum (5.08 g, 39.5%, MS (m/e)=307.2 [M+H+]).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08729061B2
출처 데이터셋uspto-grants-2014_05
ORD IDord-545695dd0df944b9b559205a855afc46
출처 메모uspto-grants-2014_05