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HRID 252084作成日:2026年10月27日

2,4-Dichlorobenzaldehyde → (S)-tert-Butyl 3-((2,4-dichlorobenzyl)amino)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/252084

反応式

関与物質

役割名称HCID仕込み量
反応物2,4-DichlorobenzaldehydeHCID 13404—
反応物tert-butyl (3S)-3-aminopyrrolidine-1-carboxylateHCID 854071—
反応物Sodium borohydrideHCID 4311764—
溶媒MethanolHCID 887—
生成物(S)-tert-Butyl 3-((2,4-dichlorobenzyl)amino)pyrrolidine-1-carboxylateHCID 66854615—

反応手順

Stir a mixture of (S)-3-amino-pyrrolidine-1-carboxylic acid tert-butyl ester (15.07 g, 81.0 mmol) and 2,4-dichlorobenzaldehyde (13.46 g, 76.9 mmol) in dry methanol (250 mL) at room temperature under nitrogen overnight. Add slowly sodium borohydride (4.74 g, 125.4 mmol) and stir for 10 min. Concentrate and add 2 N NaOH (150 mL) and extract with diethyl ether. Combine the organic layers, wash with saturated aqueous sodium chloride, dry (magnesium sulfate) and concentrate to give (S)-3-(2,4-dichlorobenzylamino)-pyrrolidine-1-carboxylic acid tert-butyl ester which may be used without further purification (26.9 g, 100%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07868014B2
出典データセットuspto-grants-2011_01
ORD IDord-4d67d823c64943d4a40ecc1545da463a
出典メモuspto-grants-2011_01