戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 433035作成日:2026年10月25日

Triphenylphosphine → HCID 178431455、化合物

https://huagongshe.com/reaction/433035

反応式

関与物質

役割名称HCID仕込み量
反応物TriphenylphosphineHCID 11776—
反応物DiisopropylcarbodiimideHCID 12734—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物2,4-Dichlorophenethyl alcoholHCID 2734099—
反応物3,5-Dihydroxy-4-methylbenzoic AcidHCID 2748045—
反応物Diisopropyl azodicarboxylateHCID 5363146—
反応物BistrimethylsilylacetamidHCID 11708267—
反応物HCID 178454311HCID 178454311—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 178431455HCID 178431455—

反応手順

Rink resin (239 mg; loading 0.43 mmol/g) functionalized with Arg(Boc)2 was coupled with 106 mg of 3,5-dihydroxy-4-methylbenzoic acid in the presence of DIC (85 mg) and HOBt (90 mg) in DMF (1.5 ml). The resin was then washed and treated with a 15% solution of benzyltrimethylammonium hydroxide in DMF for 45 min. The resin was washed with DMF, 10% acetic acid in DMF, DMF and DCM and dried in vacuo for 4 h. The dried resin was washed with anhydrous THF and mixed with 145 mg (0.5 mmole) of triphenylphosphane and 25 μl of bistrimethylsilylacetamide in THF and kept at room temperature for 1 h. In a separate vial a mixture of 100 mg (0.2 mmol) of 2-(2,4-dichlorophenyl)ethanol and 100 μl of DIAD in dry THF was prepared. The reaction mixture was added to the resin which had previously been cooled in a refrigerator for 10 min. Coupling was continued at room temperature overnight. The resin was washed and dried, and the final product was cleaved off and processed as described in Example 1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06664393B2
出典データセットuspto-grants-2003_12
ORD IDord-011e9b4aaf294179b893e189ce80bcdf
出典メモuspto-grants-2003_12