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

Acetic Acid → N-[(2,5-Difluorophenyl)methylidene]hydroxylamine

HRID 2265912
노트
인쇄 미리보기

반응식

HRID 2265912 반응식
[F:1][C:2]1[CH:9]=[CH:8][C:7]([F:10])=[CH:6][C:3]=1[CH:4]=O.Cl.[NH2:12][OH:13].[OH-].[Na+].C(O)(=O)C>CCO.O>[F:1][C:2]1[CH:9]=[CH:8][C:7]([F:10])=[CH:6][C:3]=1[CH:4]=[N:12][OH:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 176Acetic AcidHCID 14798Sodium HydroxideHCID 1376632,5-DifluorobenzaldehydeHCID 443297Hydroxyamine hydrochloride

생성물 1

HCID 57371077N-[(2,5-Difluorophenyl)methylidene]hydroxylamine수율 83.1%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 962Water

실험 절차

2,5-Difluorobenzaldehyde (28.5 g, 0.20 mol) was dissolved in 30 ml EtOH. 80 ml water, 80 g crushed ice and hydroxylamine hydrochloride (15.3 g, 0.22 mol) were added. 250 ml (0.50 mol) 2N NaOH were added drop wise and the yellow solution was stirred for 3 hours at room temperature. The reaction mixture was neutralized to pH 6 with acetic acid. The formed suspension was diluted with water and filtered. The crystals were washed with water and dried 2 hours at 50° C. and <20 mbar to obtain the desired product as a white solid (26.1 g, 83%). MS (m/e): 156.0 (M−H+).

후처리

  1. additionwere added
  2. filtrationfiltered
  3. washThe crystals were washed with water
  4. customdried 2 hours at 50° C.

출처 및 근거

ORD 기록
ord-cf8be64000aa424bb5ae7f2eb474068b
출처 데이터셋
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07858630B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
용매
2회