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

Methanol → 2-Naphthol

HRID 1076101
노트
인쇄 미리보기

반응식

HRID 1076101 반응식
[C:1]1(=[O:7])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[CH:8]([C:10]([CH3:12])=O)=[CH2:9].CO.[OH-].[Na+]>C1C=CC=CC=1.O.CCCCCCCC[N+](C)(C)C.[Br-].[Cr]([O-])([O-])=O.[Cu+2]>[CH:2]1[C:3]2[C:4](=[CH:9][CH:8]=[CH:10][CH:12]=2)[CH:5]=[CH:6][C:1]=1[OH:7]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

9

반응물 4

HCID 887MethanolHCID 6570Methyl vinyl ketoneHCID 7967CyclohexanoneHCID 14798Sodium Hydroxide

생성물 1

HCID 86632-Naphthol수율 75%

시약·촉매·용매 4

HCID 74964Octyltrimethylammonium bromide촉매
HCID 178505374
HCID 178505374, 화합물
촉매
HCID 241Benzene용매
HCID 962Water용매2회

반응 조건

온도
80 °C

실험 절차

Next, the 46 parts by weight of the morpholine enamine of cyclohexanone was admixed with 19 parts by weight of methyl vinyl ketone in 53 parts by weight of benzene solvent and heated at reflux (80°C) for 3 hours. After the 3 hour period, the reaction mixture was cooled and treated with the solution comprising 40 parts by weight of methanol, 25 parts by weight of water and 5 parts by weight of sodium hydroxide to yield a resulting mixture which was then heated at reflux (70°C) for 2 hours and thereafter diluted with approximately 100 parts by weight of water and separated in the 2-phases. The aqueous phase was extracted with ether to yield a phase which was combined with the organic phase and thereafter distilled to obtain a product having a boiling point of from 93°-117°F at 3 millimeters Hg. The product yield comprised 73.5% (based on octalones). A gas liquid chromatographic analysis of this product showed it to include 81.6% octalone, an 8.6 mole % decalone, and 10% other cyclic materials. The resulting mixture was then agitated with 10% of its weight of copper chromite and maintained at a temperature of 250°-350°c for 4 hours to obtain a 75% yield of pure beta-naphthol.

후처리

  1. temperatureheated
  2. temperatureAfter the 3 hour period, the reaction mixture was cooled
  3. additiontreated with the solution
  4. customto yield a resulting mixture which
  5. temperaturewas then heated
  6. temperatureat reflux (70°C) for 2 hours
  7. customseparated in the 2-phases
  8. extractionThe aqueous phase was extracted with ether
  9. customto yield a phase which
  10. distillationdistilled
  11. customto obtain a product
  12. customof from 93°-117°F
  13. customThe product yield comprised 73.5% (based on octalones)
  14. temperaturemaintained at a temperature of 250°-350°c for 4 hours

출처 및 근거

ORD 기록
ord-f821922da70e4bd9a8b89b82ca31043f
출처 데이터셋
uspto-grants-1976_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03954890

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트