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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 470605생성일: 2026년 10월 26일

Sodium hydride → HCID 136413210, 화합물

https://huagongshe.com/reaction/470605

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물3-[3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-phenyl]-acrylic Acid Methyl EsterHCID 67396155—
반응물HCID 178449909HCID 178449909—
용매TetrahydrofuranHCID 8028—
생성물HCID 136413210HCID 136413210—

반응 단계

A solution of N-hydroxy-butyramidine (0.24 g, 2.34 mmol) in tetrahydrofuran (5 mL) was added slowly into the suspension of 60% sodium hydride (0.14 g, 3.5 mmol) in dry tetrahydrofuran (5 mL) under nitrogen atmosphere at 0° C. to 10° C. The mixture was stirred for 30 min at room temperature. 3-[3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-phenyl]-acrylic acid methyl ester (compound of Example 1, Step 1; 0.5 g, 1.18 mmol) in dry tetrahydrofuran (5 mL) was added into the reaction mixture and heated at 60° C. for 8 h. The reaction mixture was cooled at 0° C. and quenched with methanol (2 mL) to destroy excess sodium hydride. The reaction mixture was extracted with ethyl acetate (2×10 mL) and the combined organic layers were washed with water (2×10 mL) followed by brine (10 mL). The organic phase obtained was dried over anhydrous sodium sulphate and concentrated to dryness. The crude product obtained was purified by column chromatography (silica gel, chloroform-methanol) to afford the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08629277B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-4c664d48321d4babab4ca34308e1347e
출처 메모uspto-grants-2014_01