반응 #6406

반응 방정식

chloroacetone

1,1-dichloroacetone

mesityl oxide

Phenol

chloroacetone

chloroacetone

sulfuric acid

→

4,4'-Dihydroxy-alphamethylstilbene

용매

acetone

water

methylene chloride

water

water

반응 조건

후처리

1. 1
   온도so as to maintain the reaction temperature between -11° C. and -9° C
2. 2
   기타After 150 minutes of post reaction between a -11° C. to -9° C. temperature range
3. 3
   기타The oil product is separated
4. 4
   세척then washed with a second portion (1000 milliliters)
5. 5
   기타After separation
6. 6
   workup.ADDITIONthe recovered oil product is added to a pair of 2 liter beakers along with ethanol (250 milliliters)
7. 7
   workup.STIRRINGstirred
8. 8
   기타to provide solutions
9. 9
   온도heating commences
10. 10
    온도As the temperature of the mixture increases
11. 11
    온도heating
12. 12
    기타reaches 90° C.
13. 13
    기타a massive precipitation of white crystalline plates
14. 14
    기타The oil layer is recovered by decantation of the water layer and ethanol (250 milliliters)
15. 15
    workup.ADDITIONis added
16. 16
    workup.ADDITIONDeionized water is again added to the stirred solutions
17. 17
    온도as heating commences
18. 18
    기타reaches 70° C.
19. 19
    기타a massive precipitation of white crystalline plates
20. 20
    workup.STIRRINGAt this time, stirring
21. 21
    workup.ADDITIONsufficient deionized water is added
22. 22
    온도the crystalline slurries are chilled to 4° C.
23. 23
    여과The crystalline product is recovered by filtration of the chilled crystalline slurries
24. 24
    workup.ADDITIONadded to a beaker along with deionized water (1000 milliliters)
25. 25
    workup.STIRRINGstirred
26. 26
    온도with heating to 100° C
27. 27
    온도After maintaining the stirred slurry at 100° C. for thirty minutes
28. 28
    여과the crystalline product is recovered by filtration
29. 29
    workup.STIRRINGstirred
30. 30
    온도with heating to 100° C
31. 31
    여과The crystalline product is recovered by filtration
32. 32
    기타then dried in a vacuum oven at 1000° C.

실험 절차

Phenol (752.8 grams, 8.0 moles), chloroacetone (384.77 grams, 4.0 moles as chloroacetone) and methylene chloride (600 grams) are added to a reactor and cooled to -10° C. with stirring under a nitrogen atmosphere. The chloroacetone used is a commercial grade containing 96.25% chloroacetone, 0.05% acetone, 3.05% 1,1-dichloroacetone and 0.60% mesityl oxide. Concentrated sulfuric acid (392.32 grams, 4.0 moles) is added dropwise to the stirred solution over a forty minute period and so as to maintain the reaction temperature between -11° C. and -9° C. After 150 minutes of post reaction between a -11° C. to -9° C. temperature range, the viscous, orange colored oil product is mixed with iced deionized water (1000 milliliters). The oil product is separated then washed with a second portion (1000 milliliters) and then a third portion (1000 milliliters) of deionized water. After separation, the recovered oil product is added to a pair of 2 liter beakers along with ethanol (250 milliliters) and stirred to provide solutions. Deionized water (250 milliliters) is added to the stirred solutions and heating commences. As the temperature of the mixture increases, the stirred mixture begins to clear. Each time clearing is observed, sufficient deionized water is added to induce cloudiness, followed by continuation of the mixing and heating. Once the temperature reaches 90° C., a massive precipitation of white crystalline plates occurs and is followed by immediate coalesence of the precipitated product to an oil. The oil layer is recovered by decantation of the water layer and ethanol (250 milliliters) is added. Deionized water is again added to the stirred solutions as heating commences, in an amount sufficient to induce cloudiness each time clearing is observed. Once the temperature reaches 70° C., a massive precipitation of white crystalline plates again occurs. At this time, stirring is stopped, sufficient deionized water is added to fill both of the beakers and the crystalline slurries are chilled to 4° C. and held therein for 16 hours. The crystalline product is recovered by filtration of the chilled crystalline slurries, added to a beaker along with deionized water (1000 milliliters), then stirred with heating to 100° C. After maintaining the stirred slurry at 100° C. for thirty minutes, the crystalline product is recovered by filtration then again combined with deionized water (1000 milliliters) and stirred with heating to 100° C. The crystalline product is recovered by filtration then dried in a vacuum oven at 1000° C. and 5 mm Hg to a constant weight of 478.8 grams. Proton magnetic resonance spectroscopy and infrared spectrophotometric analysis confirm the product structure.

출처