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

Water → HCID 15008723, 화합물

HRID 1356648
노트
인쇄 미리보기

반응식

HRID 1356648 반응식
[O:1]([NH2:3])[CH3:2].[C:4]1([CH3:14])[CH:9]=[CH:8][C:7]([S:10](Cl)(=[O:12])=[O:11])=[CH:6][CH:5]=1.O>N1C=CC=CC=1>[CH3:2][O:1][NH:3][S:10]([C:7]1[CH:8]=[CH:9][C:4]([CH3:14])=[CH:5][CH:6]=1)(=[O:12])=[O:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 4113O-MethylhydroxylamineHCID 73974-Toluenesulfonyl chloride

생성물 1

HCID 15008723HCID 15008723, 화합물수율 99%

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

Methoxylamine (9.00 g (108 mmol) was suspended in pyridine (30.0 ml). To this, under cooling with ice and with stirring, p-toluenesulfonyl chloride (19.07 g (100 mmol)) was added and the mixture was stirred under cooling with ice for 30 minutes and at room temperature for 2 hours. Water (200.0 ml) was added to the reaction mixture to bring about separation of crystals. After 30 minutes' stirring, the crystals were filtered and washed to give 20.26 g (99%) of N-methoxy-p-toluenesulfonamide as white crystals.

후처리

  1. temperatureTo this, under cooling with ice
  2. stirringthe mixture was stirred
  3. customto bring about separation of crystals
  4. stirringAfter 30 minutes' stirring
  5. filtrationthe crystals were filtered
  6. washwashed

출처 및 근거

ORD 기록
ord-745b4fe52e6c4dfd96c8ce9974edb68f
출처 데이터셋
uspto-grants-2003_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06586617B1

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트