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

Hydrochloric Acid → 2-Methyl-4-methoxy-5-nitrophenol

HRID 2050750
노트
인쇄 미리보기

반응식

HRID 2050750 반응식
S([O:5][C:6]1[CH:11]=[C:10]([N+:12]([O-:14])=[O:13])[C:9]([O:15][CH3:16])=[CH:8][C:7]=1[CH3:17])(=O)(=O)C.[OH-].[Na+].Cl>CO.O>[CH3:17][C:7]1[CH:8]=[C:9]([O:15][CH3:16])[C:10]([N+:12]([O-:14])=[O:13])=[CH:11][C:6]=1[OH:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 198211562-Methyl-4-methoxy-5-nitrophenyl mesylate

생성물 1

HCID 199401542-Methyl-4-methoxy-5-nitrophenol수율 100%

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매2회

실험 절차

In 110 ml of methanol was dissolved 15.5 g (59.4 mmol) of 2-methyl-4-methoxy-5-nitrophenyl mesylate. Then 6.5 g of sodium hydroxide dissolved in 20 ml of water was added thereto. The obtained mixture was heated under reflux for 1 hour. After cooling, concentrated hydrochloric acid was added to thereby acidify the mixture. Then 400 ml of water was added and crystals were precipitated. The crystals were collected by filtration and washed with water. Thus 10.9 g (59.4 mmol) of 2-methyl-4-methoxy-5-nitrophenol was obtained. The yield was 100%.

후처리

  1. additionwas added
  2. temperatureThe obtained mixture was heated
  3. temperatureunder reflux for 1 hour
  4. temperatureAfter cooling
  5. customcrystals were precipitated
  6. filtrationThe crystals were collected by filtration
  7. washwashed with water

출처 및 근거

ORD 기록
ord-f72d44e6a4f64d369075518aaaa7be56
출처 데이터셋
uspto-grants-1991_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05015260

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트