Epichlorohydrin → HCID 73851539, compound

HRID 856872

Reaction equation

HRID 856872 reaction equation
[C:1]1([N:7]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[N:8]=[CH:9][C:10]2[CH:15]=[CH:14][C:13]([N:16]([CH2:19][CH3:20])[CH2:17][CH3:18])=[CH:12][C:11]=2[OH:21])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH-].[K+].S([O-])([O-])(=O)=O.[Na+].[Na+].[CH2:37]([CH:39]1[O:41][CH2:40]1)Cl>C(OCC)C>[C:1]1([N:7]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[N:8]=[CH:9][C:10]2[CH:15]=[CH:14][C:13]([N:16]([CH2:19][CH3:20])[CH2:17][CH3:18])=[CH:12][C:11]=2[O:21][CH:40]2[O:41][CH:39]2[CH3:37])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1

Participants

6

Reactant 4

HCID 7835EpichlorohydrinHCID 14797Potassium HydroxideHCID 24436Sodium SulfateHCID 33912063-(Diethylamino)-6-[(2,2-diphenylhydrazinyl)methylidene]-1-cyclohexa-2,4-dienone2×

Product 1

HCID 73851539HCID 73851539, compoundYield 77.6%

Reagents, catalysts & solvents 1

HCID 3283Diethyl EtherSolvent

Procedure

A mixture of the 4-diethylamino-2-hydroxybenzaldehyde N,N-diphenylhydrazone (10.0 g, 27.82 mmol, prepared as described above), 85% powdered potassium hydroxide (3.7 g, 0.05 mol), and anhydrous sodium sulfate (1.4 g, 11.13 mmol) in 35 ml of epichlorohydrin (commercially obtained from Aldrich, Milwaukee, Wis.) was stirred vigorously at 30–35° C. until the 4-diethylamino-2-hydroxybenzaldehyde N,N-diphenylhydrazone disappeared (2.5 hours, as determined by thin layer chromatography (TLC)). After termination of the reaction by cooling the mixture to room temperature, the mixture was diluted with diethyl ether, and washed with copious amounts of water until the washed water reached a pH value of 7. The organic layer was dried over anhydrous magnesium sulfate, treated with activated charcoal, and filtered. The diethyl ether and unreacted epichlorohydrin were removed by evaporation under a vacuum. The crystals formed upon standing at room temperature were filtered off and washed with 2-propanol to give 9.0 g (77.6%) of the desired compound. The melting point was found to be 86–87° C. (recrystallized from 10:1 v/v of 2-propanol:ether mixture). The 1H NMR spectrum (100 MHz) of the product in CDCl3 was characterized by the following chemical shifts (δ, ppm): 8.0 (d, 1H, 6-H of 1,2,4-subst. Ph); 7.8–7.0 (m, 11H, CH═N, Ph); 6.45 (d, 1H, 5-H of 1,2,4-subst. Ph); 6.1 (s, 1H, 3-H of 1,2,4-subst. Ph); 4.35–3.75 (m, 2H, OCH2); 3.35 (q, 4H, CH2); 3.05 (p, 1H, CH); 3.65 (t, 1H, one of CH2 of oxirane); 2.45 (dd, 1H, one of CH2 of oxirane); 1.15 (t, 6H, CH3). Elemental analysis yielded the following values in weight percent C, 74.95; H, 6.88; and N, 9.92; which compared with calculated values for C26H29N3O2 in weight percent of C, 75.15; H, 7.03; and N, 10.11.

Workup

  1. custom(2.5 hours, as determined by thin layer chromatography (TLC))
  2. customAfter termination of the reaction
  3. washwashed with copious amounts of water until the washed water
  4. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  5. additiontreated with activated charcoal
  6. filtrationfiltered
  7. customThe diethyl ether and unreacted epichlorohydrin were removed by evaporation under a vacuum
  8. customThe crystals formed
  9. customupon standing at room temperature
  10. filtrationwere filtered off
  11. washwashed with 2-propanol

Sources & evidence

ORD record
ord-a7ed02fb8bda476b9503c239dd20a26e
Source dataset
uspto-grants-2006_12
Patent number
US07144665B2

Linked notes

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