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HRID 1489218作成日:2026年10月25日

Acetic Acid → Benzenemethanamine, N-ethyl-4-methoxy-

https://huagongshe.com/reaction/1489218

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物EthylamineHCID 6341—
反応物4-MethoxybenzaldehydeHCID 31244—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒1,2-DichloroethaneHCID 11—
溶媒MethanolHCID 887—
溶媒DichloromethaneHCID 6344—
生成物Benzenemethanamine, N-ethyl-4-methoxy-HCID 29601859%

反応手順

To a mixture of anisaldehyde (15.6 g, 115 mmol) and ethylamine (2.0M in THF, 87 mL, 174 mmol) in 1,2-dichloroethane (450 mL) was added glacial acetic acid (10.0 mL, 174 mmol) under nitrogen atmosphere. The reaction mixture was stirred at room temperature for 30 min and then cooled to 0° C. with ice bath. NaBH(OAc)3 (36.9 g, 174 mmol) was added portionwise and the reaction mixture was stirred at room temperature overnight. The mixture was concentrated and the residue was diluted with a basic solution (10 g NaOH in 100 mL of water) to make the solution slightly basic. This aqueous layer was extracted with ether. The combined extracts were washed with water, brine, dried and concentrated. The residue was chromatographed on silica gel (elution with 5% MeOH in CH2Cl2 and then 50% MeOH in CH2Cl2 containing 4% Et3N) to afford the product (11.2 g, 59% yield) as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05677346
出典データセットuspto-grants-1997_10
ORD IDord-fa44be8f287941c6adc3185b2063bd59
出典メモuspto-grants-1997_10