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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1741415생성일: 2026년 10월 26일

Potassium Hydroxide → 1-[2-[4,5-Bis(4-methylphenyl)oxazol-2-yl]pyrrolidin-1-yl]-1,2,3,4-tetrahydro-5-t-butyldiphenylsilyloxynaphthalene

https://huagongshe.com/reaction/1741415

반응식

참여 물질

역할이름HCID투입량
반응물Potassium HydroxideHCID 14797—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물1,2,3,4-Tetrahydro-5-t-butyldiphenylsilyloxy-1-naphthaleneamineHCID 18367231—
반응물1-[4,5-Bis(4-methylphenyl)oxazol-2-yl)butan-1,4-dioneHCID 18367347—
용매Acetic AcidHCID 176—
용매MethanolHCID 887—
생성물1-[2-[4,5-Bis(4-methylphenyl)oxazol-2-yl]pyrrolidin-1-yl]-1,2,3,4-tetrahydro-5-t-butyldiphenylsilyloxynaphthaleneHCID 1836724294.8%

반응 단계

A solution of 1,2,3,4-tetrahydro-5-t-butyldiphenylsilyloxy-1-naphthaleneamine (0.21 g), 1-[4,5-bis(4-methylphenyl)oxazol-2-yl)butan-1,4-dione (0.12 g), NaBH3CN (84 mg) and KOH (30 mg) in acetic acid (0.5 ml) and methanol (4 ml). After being stirred for 3 days at room temperature, the solvent was evaporated in vacuo. The residue was partitioned between ethyl acetate and sat. NaHCO3. The organic layer was washed with brine. The dried solvent was evaporated in vacuo. The residue was purified by chromatography on silica gel to give 1-[2-[4,5-bis(4-methylphenyl)oxazol-2-yl]pyrrolidin-1-yl]-1,2,3,4-tetrahydro-5-t-butyldiphenylsilyloxynaphthalene (0.24 g). FABMS (m/z): 702 (M+ -1) NMR (CDCl3, δ): 1.08 (9H, s), 1.58-3.04 (12H, m), 2.34 (3H, s), 2.36 (3H, s), 6.18-7.80 (21H, m)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05972965
출처 데이터셋uspto-grants-1999_10
ORD IDord-f18da2ce4fbe40ddb55e49c0bac305d2
출처 메모uspto-grants-1999_10