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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1489218생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1489218

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물EthylamineHCID 6341—
반응물4-MethoxybenzaldehydeHCID 31244—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매1,2-DichloroethaneHCID 11—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
생성물Benzenemethanamine, N-ethyl-4-methoxy-HCID 29601859%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05677346
출처 데이터셋uspto-grants-1997_10
ORD IDord-fa44be8f287941c6adc3185b2063bd59
출처 메모uspto-grants-1997_10