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HRID 896755作成日:2026年10月26日

Diisopropylethylamine → Retinol phosphoramidite

https://huagongshe.com/reaction/896755

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物RetinolHCID 445354—
反応物Sodium BicarbonateHCID 516892—
反応物PhosphoramiditeHCID 10080320—
溶媒MethanolHCID 887—
溶媒DichloromethaneHCID 6344—
溶媒TriethylamineHCID 8471—
生成物Retinol phosphoramiditeHCID 131722191—

反応手順

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-diiso-ropylchlorophosphoramidate (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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06919439B2
出典データセットuspto-grants-2005_07
ORD IDord-3baf4227016e4a6e994874a95370b550
出典メモuspto-grants-2005_07