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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 486670생성일: 2026년 10월 25일

Acetic Anhydride → N-acetyl-2-amino-N-methyl-alpha-(3-methyl-2-thienyl)benzeneethanamine

https://huagongshe.com/reaction/486670

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물Compound 7189HCID 130176—
용매PyridineHCID 1049—
생성물N-acetyl-2-amino-N-methyl-alpha-(3-methyl-2-thienyl)benzeneethanamineHCID 2241444750.5%

반응 단계

A stirred, ice water chilled solution of 5.07 g of 2-amino-N-methyl-α-(3-methyl-2-thienyl)benzeneethanamine in 40 ml of pyridine was treated dropwise with 2.25 g of acetic anhydride. The solution was stirred with cooling for 15 minutes and then at room temperature for 3 hours. After standing overnight, the reaction mixture was decanted into water (200 ml), treated with dichloromethane (100 ml) and basified with 10% sodium hydroxide solution. The aqueous phase was extacted with dichloromethane (150 ml), and the combined organic phase was filtered and concentrated. The resulting solid was stirred with toluene and evaporated to dryness. Recrystallization from propionitrile (14 ml) afforded 3.0 g of N-acetyl-2-amino-N-methyl-α-(3-methyl-2-thienyl)benzeneethanamine, mp 176°-181.5° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05292760
출처 데이터셋uspto-grants-1994_03
ORD IDord-6904f10396fd43aba71c444b02a81509
출처 메모uspto-grants-1994_03