Tetrahydrofuran → Cyclohexanone

HRID 1081556Notes

Reaction equation

HRID 1081556 reaction equation
[C:1]([C:3]([C:9]1[CH:23]=[CH:22][C:12]([N:13]([CH2:18][CH2:19][CH2:20][CH3:21])[CH2:14][CH2:15][CH2:16][CH3:17])=[CH:11][CH:10]=1)=[C:4]([C:7]#[N:8])[C:5]#[N:6])#[N:2].[O:24]1CCCC1>C(C(C)=O)C>[C:9]1(=[O:24])[CH2:23][CH2:22][CH2:12][CH2:11][CH2:10]1.[C:1]([C:3]([C:9]1[CH:23]=[CH:22][C:12]([N:13]([CH2:18][CH2:19][CH2:20][CH3:21])[CH2:14][CH2:15][CH2:16][CH3:17])=[CH:11][CH:10]=1)=[C:4]([C:5]#[N:6])[C:7]#[N:8])#[N:2]

Participants

5

Procedure

A dye solution containing 3.37 wt-% dibutyl magenta dye (4-tricyanovinyl-N,N-dibutylaniline), 0.84 wt-% butyl magenta (structure shown below), 3.94 wt-% GEON® 178 (polyvinyl chloride, B.F. Goodrich Co., Cleveland, Ohio), 0.28 wt-% VITEL™ PE-200 (polyester resin from Goodyear Chemicals Co., Akron, Ohio), 1.57 wt-% TROYSOL™ CD 1 dispersing agent (CAS registry No.: 64742-88-7, purchased from Troy Chemical, Newark, N.J.), 13.5 wt-% tetrahydrofuran, 36.0 wt-% methyl ethyl ketone, and 40.5 wt-% cyclohexanone was prepared. The individual components were first dissolved in an appropriate solvent and then mixed. ##STR1## This dye solution was coated onto the antistatic layer using a No. 9 Mayer bar and dried at 85° C. for five minutes to give an antistatic thermal dye transfer donor film. The static decay time for the antistatic thermal dye transfer donor film was 0.04 second. In comparison, the dye solution was applied to unprimed and untreated 5.7 micron Teijin F22G polyester film using a No. 9 Mayer bar and dried at 85° C. for 5 minutes to give a non-antistatic thermal dye transfer film. The non-antistatic film did not exhibit decay of a triboelectrically generated charge and could not be charged by the Electro-tech Static Decay Meter.

Workup

  1. dissolutionThe individual components were first dissolved in an appropriate solvent
  2. additionmixed
  3. custom9 Mayer bar and dried at 85° C. for five minutes

Sources & evidence

ORD record
ord-8c6598b7877b435f8c4d054e2b89e7d5
Source dataset
uspto-grants-1996_12
Patent number
US05587351

Reaction notes

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