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HRID 60250作成日:2026年10月26日

Formaldehyde → (R)-tert-butyl 3-(hydroxymethyl)-4-methylpiperazine-1-carboxylate

https://huagongshe.com/reaction/60250

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物Sodium CarbonateHCID 10340—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物tert-Butyl (3R)-3-(hydroxymethyl)piperazine-1-carboxylateHCID 24820286—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
溶媒DichloromethaneHCID 6344—
生成物(R)-tert-butyl 3-(hydroxymethyl)-4-methylpiperazine-1-carboxylateHCID 58365052—

反応手順

To a solution of (R)-tert-butyl 3-(hydroxymethyl)piperazine-1-carboxylate (115 mg, 0.53 mmol) in acetonitrile (1.4 mL) and water (0.3 mL) was added Formalin (0.11 mL, 1.6 mmol) followed by sodium triacetoxyborohydride (225 mg, 1.1 mmol). The reaction mixture was stirred for 20 minutes at ambient temperature. The reaction mixture was then basified via the addition of saturated aqueous sodium carbonate solution (1 mL), diluted with methylene chloride (50 mL) and methanol (5 mL), and washed with saturated aqueous sodium bicarbonate solution (2×15 mL). The organic layer was separated, dried over sodium sulfate, and concentrated in vacuo to afford a white crystalline solid, which was used in the next step without any further purification (120 mg, 98%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09440976B2
出典データセットuspto-grants-2016_09
ORD IDord-209d4574534a4c8dbaebce40c777f396
出典メモuspto-grants-2016_09