Methanol → HCID 13548209, compound

HRID 259064

Reaction equation

HRID 259064 reaction equation
[CH2:1]([NH:3][C:4](=[O:7])[CH2:5][CH3:6])[CH3:2].[CH3:8][OH:9]>F[B-](F)(F)F.C[N+](C)(C)C>[CH3:8][O:9][CH:1]([NH:3][C:4](=[O:7])[CH2:5][CH3:6])[CH3:2]

Participants

4

Conditions

Temperature
40 °C

Procedure

36.9 g of methanol was charged into an electrolysis cell according to Example 5, wherein 0.37 g of tetramethyl ammonium tetrafluoroborate were dissolved as conducting salt. After switching on the electrolysis current, the anode current density was 2 A/dm2. The temperature was maintained at 40° C. during the electrolysis. Agitation was performed by a magnetic stirrer at from 30 to 35 revolutions per minute. After the passage of a current quantity of 4.06 Faraday per mole of N-ethylpropionic acid amide, the current was switched off. The calculated average cell tension was 54.9 volts. After work up of the electrolysis solution in known manner there were obtained 24.4 g of N-(α-methoxyethyl)-propionic acid amide (melting point 29°-32° C., nD35 = 1.4333), representing a material efficiency of 80.7% and a current efficiency of 40.4%.

Workup

  1. dissolutionwere dissolved
  2. customAgitation was performed by a magnetic stirrer at from 30 to 35 revolutions per minute

Sources & evidence

ORD record
ord-850328cdc20b4862a652035f9d5df1b5
Source dataset
uspto-grants-1977_07
Patent number
US04036712

Linked notes

Loading…