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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → 2-methyl-4-(trifluoromethyl)aniline hydrochloride

HRID 857586
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인쇄 미리보기

반응식

HRID 857586 반응식
[CH3:1][C:2]1[CH:7]=[C:6]([C:8]([F:11])([F:10])[F:9])[CH:5]=[CH:4][C:3]=1[NH:12]C(=O)C.[ClH:16].CC1C=C(C(F)(F)F)C=CC=1N>C(O)C>[ClH:16].[CH3:1][C:2]1[CH:7]=[C:6]([C:8]([F:9])([F:10])[F:11])[CH:5]=[CH:4][C:3]=1[NH2:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 2783135N-[2-methyl-4-(trifluoromethyl)phenyl]acetamideHCID 137504374-Amino-3-methylbenzotrifluoride

생성물 1

HCID 218690732-methyl-4-(trifluoromethyl)aniline hydrochloride

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A solution of N-[2-methyl-4-(trifluoromethyl)phenyl]acetamide (5.17 g) and aqueous hydrochloric acid (37%, 12 mL) in ethanol (24 mL) was heated to reflux for 3 hours and then stirred at ambient temperature for 48 hours. GC analysis of the reaction mixture showed a 98:2 peak area ratio of 2-methyl-4-(trifluoromethyl)aniline to starting material. 2-Methyl-4-(trifluoromethyl)aniline hydrochloride was obtained as a white solid by filtering the reaction mixture and washing the solids with ethyl acetate. A second crop of 2-methyl-4-(trifluoromethyl)aniline hydrochloride was obtained by evaporating the filtrate to dryness, triturating the residue in ethyl acetate, then filtering, providing a total of 4.27 g (85% yield).

후처리

  1. temperatureto reflux for 3 hours

출처 및 근거

ORD 기록
ord-d921fd13fd9a4c008a064028f57cdc02
출처 데이터셋
uspto-grants-2006_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07145035B2

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