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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Anhydride | HCID 7918 | — |
| 반응물 | Compound 7189 | HCID 130176 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | N-acetyl-2-amino-N-methyl-alpha-(3-methyl-2-thienyl)benzeneethanamine | HCID 22414447 | 50.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05292760 |
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| 출처 데이터셋 | uspto-grants-1994_03 |
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| ORD ID | ord-6904f10396fd43aba71c444b02a81509 |
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| 출처 메모 | uspto-grants-1994_03 |
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