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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1828생성일: 2026년 10월 24일

tert-Butanol → 2-Tert-butoxycarbonylamino-6,11-dihydrodibenz[b,e]oxepin-11-one

https://huagongshe.com/ko/reaction/1828

반응식

참여 물질

역할이름HCID투입량
반응물tert-ButanolHCID 6386—
반응물TriethylamineHCID 8471—
반응물P,P-Diphenylphosphinic azideHCID 199401—
반응물Sodium BicarbonateHCID 516892—
반응물Olopatadine Impurity 17HCID 12446821—
생성물2-Tert-butoxycarbonylamino-6,11-dihydrodibenz[b,e]oxepin-11-oneHCID 1969301641%

반응 단계

To tert-butanol (8.3 ml) were added diphenylphosphoryl azide (1.1 ml, 5.11 mmol), 2-carboxy-6,11-dihydrodibenz-[b,e]oxepin-11-one (Japanese Published Unexamined Patent Application No. 91040/90) (1.0 g, 3.9 mmol), and triethylamine (0.71 ml, 5.11 mmol) under an atmosphere of argon gas, followed by heating under reflux for 2 hours. After the reaction mixture was cooled, it was poured into a 5% aqueous solution of sodium bicarbonate, followed by extraction with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium chloride, and then dried over anhydrous magnesium sulfate. After the drying agent was filtered off, the organic layer was concentrated under reduced pressure. The obtained oily substance was purified by silica gel column chromatography (hexane/ethyl acetate=8/1), followed by trituration with hexane to give 2-tert-butoxycarbonylamino-6,11-dihydrodibenz[b,e]oxepin-11-one as a white solid (0.51 g, 41%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726325
출처 데이터셋uspto-grants-1998_03
ORD IDord-e2a46196bcf14ceb891b2c6cabfdc4c1
출처 메모uspto-grants-1998_03