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HRID 85355作成日:2026年10月24日

Ethylenediamine → Benzyl N-(2-aminoethyl)carbamate

https://huagongshe.com/ja/reaction/85355

反応式

関与物質

役割名称HCID仕込み量
反応物EthylenediamineHCID 3301—
反応物Methanesulfonic AcidHCID 6395—
反応物Bromocresol GreenHCID 6451—
反応物Benzyl chloroformateHCID 10387—
反応物HCID 178476685HCID 178476685—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物Benzyl N-(2-aminoethyl)carbamateHCID 279425751%

反応手順

Ethylenediamine (1.0 g, 16.7 mmol) is dissolved in water (3.0 mL) containing bromocresol green as an indicator. Methane sulfonic acid (2.8 g, 31 mmol) in water (3.0 mL) is added until a blue to pale yellow color transition is just achieved. The solution is diluted with ethanol (8.0 mL) and vigorously stirred. To the mixture was added the solution of Cbz-Cl (2.8 g, 16.7 mmol) in dimethoxyethane (4 mL) and 50% w/v aqueous AcOK (10 mL) at 20° C. simultaneously to maintain the pale yellow-green color of the indicator. After the additions are complete the mixture was stirred (RT, 1 h) and concentrated at low temperature under vacuum to removed the volatiles. The residue was shaken with water (20 mL) and filtered. The filtrate was then washed with toluene (3×50 mL), basified with excess 40% aqueous NaOH and extracted with toluene (3×50 mL). The organic layer was washed with brine (50 mL), dried over Na2SO4 and evaporated to give benzyl 2-aminoethylcarbamate as an oil (1.65 g, 51%). Mass calculated for C10H14N2O2=194.23; found: [M−H]+=193.3.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846972B2
出典データセットuspto-grants-2014_09
ORD IDord-4a860e4ef292473a9a0e191aba6087bb
出典メモuspto-grants-2014_09