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HRID 73296作成日:2026年10月24日

Diethanolamine → 2-Butyl-1,3,6,2-dioxazaborocane

https://huagongshe.com/ja/reaction/73296

反応式

関与物質

役割名称HCID仕込み量
反応物DiethanolamineHCID 8113—
反応物Butylboronic AcidHCID 20479—
反応物N,N,N',N'-Tetramethyl-L-tartramideHCID 6610750—
溶媒DichloromethaneHCID 6344—
溶媒Sodium chloride; waterHCID 57417360—
生成物2-Butyl-1,3,6,2-dioxazaborocaneHCID 346607—

反応手順

2-(But-1-yl)-tetrahydro-4H-1,3,6,2-dioxazaborocine [CAS 92527-13-4] (3 g, 17.5 mmol), which was prepared from n-butylboronic acid and 2-(2-hydroxy-ethylamino)-ethanol [CAS 111-42-2] as reported in Organic Synthesis, 1998, 76, 86-96, and (2R,3R)-2,3-dihydroxy-N,N,N′,N′-tetramethyl-butanediamide [CAS 26549-65-5] (9.85 g) were dissolved in anhydrous dichloromethane (160 mL) under N2, Brine (25 mL) was added. The resulting mixture was stirred at room temperature for about 16 hours. The two layers were separated, and the aqueous layer was extracted with dichloromethane. The combined organic layers were washed with 50 mL brine, dried over MgSO4, filtered and concentrated in vacuo to provide the title compound as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08829041B2
出典データセットuspto-grants-2014_09
ORD IDord-5e1ec3aea6574a1d88a733e20de2ceb7
出典メモuspto-grants-2014_09