1-Butanol → 1-Butene, 3-butoxy-

HRID 1276843Notes

Reaction equation

HRID 1276843 reaction equation
[CH2:1]([OH:5])[CH2:2][CH2:3][CH3:4].[CH2:6]=[CH:7][CH:8]=[CH2:9]>>[CH2:1]([O:5][CH:8]([CH3:9])[CH:7]=[CH2:6])[CH2:2][CH2:3][CH3:4].[CH2:1]([O:5][CH2:6][CH:7]=[CH:8][CH3:9])[CH2:2][CH2:3][CH3:4]

Participants

4

Procedure

A 0.3 1 stirred autoclave was filled with 67.0 g (0.90 mol) of n-butanol and with 11.5 g of Lewatit® SPC 118 in the H+ form, which had been washed beforehand with water and n-butanol, and with 3.5 g of a Lewatit® SPC 118 ion exchanger doped with copper(II) chloride. 47.0 g (0.88 mol) of 1,3-butadiene were then forced into the autoclave. After reaction for 10 hours at 90° C. and under autogeneous pressure, a selectivity of 46.8% for 3-butoxybut-1-ene and a selectivity of 44.3% for 1-butoxybut-2-ene (based on butadiene) were obtained at a conversion of 69.1%.

Workup

  1. washhad been washed beforehand with water and n-butanol
  2. customAfter reaction for 10 hours at 90° C.

Sources & evidence

ORD record
ord-211bc0a76f214a8886ba56ff1f4a5072
Source dataset
uspto-grants-2000_12
Patent number
US06166265

Reaction notes

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