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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1244751생성일: 2026년 10월 23일

Diisopropylethylamine → Retinol phosphoramidite

https://huagongshe.com/ko/reaction/1244751

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물RetinolHCID 445354—
반응물Sodium BicarbonateHCID 516892—
반응물PhosphoramiditeHCID 10080320—
반응물2-Cyanoethyl-n,n-diisopropylchlorophosphoramidateHCID 15927910—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
용매TriethylamineHCID 8471—
생성물Retinol phosphoramiditeHCID 131722191—

반응 단계

All-trans-retinol (1 g) was vacuum dried and dissolved in anhydrous CH2Cl2 (10 ml) in an argon atmosphere. Diisopropylethylamine (2.65 ml, 21.5 mmol) was syringed in and the reaction mixture was cooled in an ice-bath. 2-cyanoethyl-N,N-diisopropylchlorophosphoramidate (2.5 g, 2.45 ml, 10.5 mmol) was slowly added by syringe under argon atmosphere. The reaction mixture was stirred for 30 min. at which time TLC (CH2Cl2:CH3OH:Et3N, 90:10:0.1) indicated complete conversion of the alcohol to its phosphoramidite. The reaction mixture was added to 100 ml of saturated NaHCO3 followed by washing the reaction flask with (2×25 ml) CH2Cl2. The CH2Cl2 layer was separated and washed with 100 ml of saturated NaCl solution and dried over anhydrous MgSO4 and evaporated into a yellow foam. The amidite was used directly in the DNA synthesizer without further purification since decomposition of this amidite was noted upon silica column purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07122649B2
출처 데이터셋uspto-grants-2006_10
ORD IDord-f9d8db6e4ab94da683052f52397a2358
출처 메모uspto-grants-2006_10