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HRID 540856作成日:2026年10月25日

tert-butyl N-(4-aminobutyl)carbamate → Tert-butyl[4-(methanesulfonylamino)butyl]carbamate

https://huagongshe.com/reaction/540856

反応式

関与物質

役割名称HCID仕込み量
反応物tert-butyl N-(4-aminobutyl)carbamateHCID 4351—
反応物TriethylamineHCID 8471—
反応物Methanesulfonyl chlorideHCID 31297—
溶媒Acetic AcidHCID 176—
生成物Tert-butyl[4-(methanesulfonylamino)butyl]carbamateHCID 5418089996.7%

反応手順

Under a nitrogen atmosphere, a solution of tert-butyl N-(4-aminobutyl)carbamate (13.8 g, 73.4 mmol) and triethylamine (15.3 mL, 110 mmol) was cooled to 0° C. Methanesulfonyl chloride (6.3 mL, 81 mmol) was added, and the reaction was allowed to warm to ambient temperature and stirred overnight. Aqueous acetic acid (200 mL of 10%) was added. The organic layer was then separated and washed with water (200 mL), saturated aqueous sodium bicarbonate (200 mL), water (200 mL), and brine; dried over sodium sulfate, filtered, and concentrated under reduced pressure to provide 18.9 g of tert-butyl[4-(methanesulfonylamino)butyl]carbamate as an off-white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08871782B2
出典データセットuspto-grants-2014_10
ORD IDord-234abd4122134a918ea109f9fcf648ed
出典メモuspto-grants-2014_10