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

1-Propanol → HCID 178459131, 화합물

HRID 233126
노트
인쇄 미리보기

반응식

HRID 233126 반응식
[CH2:1]([OH:4])[CH2:2][CH3:3].C1(C)C=CC=CC=1.[O-2].[O-2].[O-2].[O-2].[O-2].[V+5:17].[V+5]>O>[O-:4][CH2:1][CH2:2][CH3:3].[V+5:17].[O-:4][CH2:1][CH2:2][CH3:3].[O-:4][CH2:1][CH2:2][CH3:3].[O-:4][CH2:1][CH2:2][CH3:3].[O-:4][CH2:1][CH2:2][CH3:3]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 10311-PropanolHCID 1140TolueneHCID 178419084HCID 178419084, 화합물

생성물 1

HCID 178459131HCID 178459131, 화합물

시약·촉매·용매 1

HCID 962Water용매

반응 조건

온도
90 °C

실험 절차

60 ml of n-propanol and 60 ml of toluene were added to 18.2 g of vanadium pentoxide. The mixture was heated to 90° C., and formed water was azeotropically removed to obtain vanadium propoxide. Here, about 60% of vanadium pentoxide was converted to vanadium propoxide. To such the reaction solution, 70 ml of isobutanol was added, and 7.2 ml of water was further added for hydrolysis, whereby a gel-like precipitate formed. Then, 200 ml of butanol and 32.8 g of 100% phosphoric acid were added thereto. The temperature was raised with stirring, and refluxing was continued to obtain a blue solid. After conducting the refluxing for 10 hours, the mixture was cooled and subjected to filtration to obtain a catalyst precursor C. The catalyst precursor C had a size and shape as shown in FIG. 8.

후처리

  1. customwas azeotropically removed

출처 및 근거

ORD 기록
ord-cce159362c2b470e809bb89206cc1209
출처 데이터셋
uspto-grants-1997_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05591870

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트