1-Propanol → HCID 178459131, compound

HRID 233126

Reaction equation

HRID 233126 reaction equation
[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]

Participants

5

Conditions

Temperature
90 °C

Procedure

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.

Workup

  1. customwas azeotropically removed

Sources & evidence

ORD record
ord-cce159362c2b470e809bb89206cc1209
Source dataset
uspto-grants-1997_01
Patent number
US05591870

Linked notes

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