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

Hexamethylenetetramine → 2-Amino-1-(4-nitrophenyl)ethan-1-one hydrochloride

HRID 1024423
노트
인쇄 미리보기

반응식

HRID 1024423 반응식
C1N2CN3CN(C2)C[N:2]1C3.Br[CH2:12][C:13]([C:15]1[CH:20]=[CH:19][C:18]([N+:21]([O-:23])=[O:22])=[CH:17][CH:16]=1)=[O:14].C(Cl)[Cl:25]>>[ClH:25].[NH2:2][CH2:12][C:13]([C:15]1[CH:20]=[CH:19][C:18]([N+:21]([O-:23])=[O:22])=[CH:17][CH:16]=1)=[O:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 4101HexamethylenetetramineHCID 6344DichloromethaneHCID 668402-Bromo-4'-nitroacetophenone

생성물 1

HCID 27928012-Amino-1-(4-nitrophenyl)ethan-1-one hydrochloride수율 72%

실험 절차

Hexamethylenetetramine (20.1 g) was added to a solution of 2-bromo-1-(4-nitrophenyl)ethanone (step A product, 25 g) in DCM (250 ml) and the mixture was stirred for 1 hour. It was then filtered and the residue was dissolved in ethanolic HCl (40 mL HCl in 162 ml EtOH). The ethanolic solution was stirred for 3 hours and was left undisturbed for 2 days. The solution was filtered and the residue was washed with water and dried to yield 11.8 g (72%) of the title compound. 1HNMR (DMSO-d6, 300 MHz): δ 8.3 (bs, 3H), 8.38 (d, 2H), 8.27 (d, 2H), 4.68 (s, 2H).

후처리

  1. filtrationIt was then filtered
  2. dissolutionthe residue was dissolved in ethanolic HCl (40 mL HCl in 162 ml EtOH)
  3. stirringThe ethanolic solution was stirred for 3 hours
  4. waitwas left undisturbed for 2 days
  5. filtrationThe solution was filtered
  6. washthe residue was washed with water
  7. customdried

출처 및 근거

ORD 기록
ord-326f391185494cec9899d74fd2f8c182
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08722901B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트