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HRID 1984966作成日:2026年10月25日

Nitrogen → (S)-Tetrahydrofuran-3-yl (3-aminobenzyl)carbamate

https://huagongshe.com/reaction/1984966

反応式

関与物質

役割名称HCID仕込み量
反応物NitrogenHCID 947—
反応物(S)-Tetrahydrofuran-3-yl (3-nitrobenzyl)carbamateHCID 57718888—
触媒PalladiumHCID 23938—
溶媒Ethyl AcetateHCID 8857—
生成物(S)-Tetrahydrofuran-3-yl (3-aminobenzyl)carbamateHCID 59901461—

反応手順

Charged 15 g of (S)-tetrahydrofuran-3-yl 3-nitrobenzylcarbamate 2c in 120 ml EtOAc to a 1 L Parr bomb at room temperature under a blanket of N2. The agitator was started and the vessel pressurized with N2 to 0.75 bar, then the pressure was released. This procedure was repeated 3 times, then the agitator was stopped before adding 0.225 g of 5% Pd/C. The agitator was started, the vessel pressurized with N2 to 0.75 bar, then the pressure was released. This procedure was repeated 3 times, then the agitator was stopped. The vessel was pressurized with H2 to 2 bar, then the pressure was released. This procedure was repeated 3 times, then the vessel was pressurized with H2 to 6.75 bar. The agitator was started and the suspension stirred until complete conversion was evident by HPLC. The H2 pressure was released, the vessel re-pressurized with N2 to 0.75 bar, then the pressure was released. This procedure was repeated 3 times then the agitator was stopped, the reaction mixture filtered through celite and the filter cake rinsed with 30 ml EtOAc to give crude (S)-tetrahydrofuran-3-yl 3-aminobenzylcarbamate 2d as a solution in EtOAc that was used as is immediately in the next step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07544810B2
出典データセットuspto-grants-2009_06
ORD IDord-2ef9ba87b3bc4365be7da63e971b94af
出典メモuspto-grants-2009_06