홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Sulfuric Acid → Ethanol, 2-((4-amino-3-methylphenyl)ethylamino)-, sulfate (1:1)

HRID 436550
노트
인쇄 미리보기

반응식

HRID 436550 반응식
[NH:1]([C:5]1[CH:16]=[CH:15][C:8]([N:9]([CH2:12][CH2:13][OH:14])[CH2:10][CH3:11])=[CH:7][C:6]=1[CH3:17])C(C)=O.C(O)(C)C.[S:22](=[O:26])(=[O:25])([OH:24])[OH:23]>>[S:22]([OH:26])([OH:25])(=[O:24])=[O:23].[NH2:1][C:5]1[CH:16]=[CH:15][C:8]([N:9]([CH2:12][CH2:13][OH:14])[CH2:10][CH3:11])=[CH:7][C:6]=1[CH3:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 1118Sulfuric AcidHCID 3776IsopropanolHCID 214528374-acetamino-3-methyl-N-(beta-hydroxyethyl)-N-ethylaniline

생성물 1

HCID 91579Ethanol, 2-((4-amino-3-methylphenyl)ethylamino)-, sulfate (1:1)

실험 절차

23.6g (0.1 mole) of 4-acetamino-3-methyl-N-(β-hydroxyethyl)-N-ethylaniline were dissolved in 30g of 50% sulfuric acid. The system was reacted for 5 hours at 80° to 100° C while stirring, and then put into 300 ml of isopropyl alcohol and stirred therein while cooling. Crystals separated out, which were then filtered and dried to obtain 22.2g of 4-amino-3-methyl-N-(β-hydroxyethyl)-N-ethylaniline sulfate.

후처리

  1. customThe system was reacted for 5 hours at 80° to 100° C
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • stirringstirred
  • temperaturewhile cooling
  • customCrystals separated out
  • filtrationwhich were then filtered
  • customdried
  • 출처 및 근거

    ORD 기록
    ord-26995c41f029417ca63be0d687a00f8c
    출처 데이터셋
    uspto-grants-1977_02
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04009205

    반응 노트

    불러오는 중…