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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 234744생성일: 2026년 10월 25일

Methanol → N-trityl-3-[4-(benzoxazol-2-yl)benzyloxy]tricyclo[3.3.1.13,7]decan-1-amine

https://huagongshe.com/reaction/234744

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물4-(Benzoxazol-2-yl)benzyl bromideHCID 11033515—
반응물N-trityl-3-hydroxytricyclo-[3.3.1.13,7]decan-1-amineHCID 54523384—
용매TetrahydrofuranHCID 8028—
생성물N-trityl-3-[4-(benzoxazol-2-yl)benzyloxy]tricyclo[3.3.1.13,7]decan-1-amineHCID 53730484—

반응 단계

To KH (35%; 0.35 g; 0.003 mole) in THF (8 ml) under N2 and cooled to 0° C. is added N-trityl-3-hydroxytricyclo-[3.3.1.13,7 ]decan-1 -amine (1 g; 0.0025 mole) of all at once. The reaction is stirred for 5 minutes with ice cooling then at room temperature for an hour, developing into a clear yellow solution. Then 4-(benzoxazol-2-yl)benzyl bromide (0.70 g; 0.0025 mole) is added and the reaction cooled in ice for 10 minutes and stirred at room temperature for 4 hours. Methanol is added to quench any KH, then the reaction is filtered and evaporated to dryness. HPLC is used to purify the product (eluting with 10% ethyl acetate/hexane) to obtain N-trityl-3-[4-(benzoxazol-2-yl)benzyloxy]tricyclo[3.3.1.13,7 ]decan-1-amine (m.p. 174°-177° C.) which is used directly in step D.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05596020
출처 데이터셋uspto-grants-1997_01
ORD IDord-826a2e324c84418a9ccc11a26eb0c153
출처 메모uspto-grants-1997_01