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HRID 1110189作成日:2026年10月26日

Triethylamine → Fmoc-Asn(Trt)-OH

https://huagongshe.com/reaction/1110189

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物N-(9-Fluorenylmethoxycarbonyloxy)succinimideHCID 134122—
反応物Potassium bisulfateHCID 516920—
反応物N-(Triphenylmethyl)-L-asparagineHCID 7408309—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物Fmoc-Asn(Trt)-OHHCID 640248—

反応手順

3.4 g of 9-fluorenylmethyl N-succinimidyl carbonate (10 mmol) are added and, at the same time, 1.4 ml of triethylamine are added dropwise so that the pH is 8.3-8.7 to a vigorously stirred solution of 3.8 g of H-Asn(Trt)-OH.0.5 H2O (10 mmol) in 20 ml of tetrahydrofuran, 10 ml of water and 1.4 ml of triethylamine (10 mmol). After 20 minutes, the mixture is cooled in an ice bath and ethyl acetate and 25 ml of a one-molar aqueous potassium bisulfate solution are added. The organic phase is washed with water until free of sulfate, dried over sodium sulfate and concentrated under reduced pressure to about 50 g. The Fmoc-Asn(Trt)-OH can be crystallized by slow addition of diisopropyl ether, m.p. 210°-211° (with decomposition).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05324833
出典データセットuspto-grants-1994_06
ORD IDord-6029d284f51645518896ddc67f84ada4
出典メモuspto-grants-1994_06