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HRID 1244751作成日:2026年10月24日

Diisopropylethylamine → Retinol phosphoramidite

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

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—
反応物2-Cyanoethyl-n,n-diisopropylchlorophosphoramidateHCID 15927910—
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-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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07122649B2
出典データセットuspto-grants-2006_10
ORD IDord-f9d8db6e4ab94da683052f52397a2358
出典メモuspto-grants-2006_10