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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 433034생성일: 2026년 10월 26일

Triphenylphosphine → HCID 178512850, 화합물

https://huagongshe.com/reaction/433034

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물DiisopropylcarbodiimideHCID 12734—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물4-Bromo-3,5-dihydroxybenzoic acidHCID 86023—
반응물2,4-Dichlorophenethyl alcoholHCID 2734099—
반응물Diisopropyl azodicarboxylateHCID 5363146—
반응물HCID 178454311HCID 178454311—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
생성물HCID 178512850HCID 178512850—

반응 단계

Rink resin (500 mg; loading 0.3 mmol/g) functionalized with Arg(Boc)2 was coupled with 176 mg of 3,5-dihydroxy-4-bromobenzoic acid in the presence of DIC (110 mg) and HOBt (78 mg) in DMF. The resin was then washed and treated with a 30% solution of benzyltrimethylammonium hydroxide in DMF for 1 h. The resin was washed with DMF, 10% acetic acid in DMF, DMF, and DCM and dried in vacuo for 3 h. The dried resin was washed with anhydrous THF and mixed with 0.2 mmol of triphenylphosphane and 0.2 mmol of 2-(2,4-dichlorophenyl)ethanol in 2 ml of dry THF. The suspension of the resin was cooled in a refrigerator for 16 min and 50 μl (0.2 mmol) of DIAD in 0.5 ml of dry THF were added. Coupling was continued overnight at room temperature. The resin was washed with dry THF and the coupling was repeated for additional 8 h. The resin was washed and dried, and the final product was cleaved off and processed as described in Example 1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06664393B2
출처 데이터셋uspto-grants-2003_12
ORD IDord-6b819f116e134274b935d0f22d796e7d
출처 메모uspto-grants-2003_12