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HRID 383770作成日:2026年10月27日

Triethylamine → tert-Butyl 3-(((methylsulfonyl)oxy)methyl)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/383770

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Methanesulfonyl chlorideHCID 31297—
反応物tert-Butyl 3-(hydroxymethyl)pyrrolidine-1-carboxylateHCID 5237175—
溶媒DichloromethaneHCID 6344—
生成物tert-Butyl 3-(((methylsulfonyl)oxy)methyl)pyrrolidine-1-carboxylateHCID 4183641—

反応手順

Mesyl chloride (106 μL, 1.37 mmol) was added to a stirred solution of tert-butyl 3-(hydroxymethyl)pyrrolidine-1-carboxylate (250 mg, 1.242 mmol) and triethylamine (225 μL, 1.62 mmol) in DCM at 0° C. After 20 min, the reaction mixture was diluted with DCM, washed with brine, dried (sodium sulfate) and concentrated in vacuo to afford the title compound i-14a. 1H NMR (500 MHz, CDCl3): δ 4.19 (m, 2H), 3.20-3.60 (m, 3H), 3.17 (m, 1H), 3.05 (s, 3H), 2.65 (m, 1H), 2.07 (m, 1H), 1.74 (m, 1H), 1.48 (s, 9H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08367679B2
出典データセットuspto-grants-2013_02
ORD IDord-7dc32f39d69c4750988ceb10a35546e6
出典メモuspto-grants-2013_02