9-Bromo-9-phenylfluorene Chemical Properties

Melting point:

99-101 °C (lit.)

Boiling point:

394.3±41.0 °C(Predicted)

Density 

1.425±0.06 g/cm3(Predicted)

storage temp. 

Keep in dark place,Sealed in dry,Room Temperature

Water Solubility 

Insoluble in water

solubility 

soluble in Chloroform, Dichloromethane, Ether, Ethyl Acetate, Methanol

form 

powder to crystal

color 

Light orange to Yellow to Green

BRN 

2561445

InChIKey

HYQXNCDBSALQLB-UHFFFAOYSA-N

CAS DataBase Reference

55135-66-5(CAS DataBase Reference)

Safety Information

Hazard Codes 

C

Risk Statements 

34

Safety Statements 

26-27-28-36/37/39-45

RIDADR 

UN 3261 8/PG 2

WGK Germany 

3

HazardClass 

8

PackingGroup 

II

HS Code 

29039930

MSDS

• Language:English Provider:9-Bromo-9-phenylfluorene
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9-Bromo-9-phenylfluorene Usage And Synthesis

Chemical Properties

Yellow Crystalline Solid

Uses

A bulky amine protecting reagent reported to be 6000 times more stable to acid than the trityl group

Uses

9-Bromo-9-phenylfluorene may be used in the preparation of:

• N-(9-(9-phenylfluorenyl))-L-alaninal
• N-(9-phenylfluoren-9-yl)-L-serine
• 1-hydroxypyrazoles priotected at the oxygen atom

General Description

Solvolysis of 9-bromo-9- phenylfluorene has been reported to proceed via limiting S_N1 mechanism.

Synthesis

(1) Prepare a 10L reactor, first add 6L of toluene, turn on the stirring; under the condition of 20-25℃, slowly add 9-phenyl-9-fluorenol (1kg, 3.87mol), stirring until completely dissolved, forming a milky white solution; (2) Slowly add 48% hydrobromic acid (2.9L, 25.5mol) to the reaction system, and the reaction solution became light yellow and showed a turbid state; (3) Place the reaction system in a water bath, heating to 50-60℃, and continue to react for 48 hours to observe the gradual deepening of the color of the reaction solution; (4) Monitor the reaction process by gas chromatography (GC). (3) The reaction system was placed in a water bath, heated to 50-60 ℃, and the reaction continued for 48 hours, observing the gradual deepening of the color of the reaction solution; (4) The reaction process was monitored by gas chromatography (GC), and the reaction was terminated when the content of the main raw material 9-phenyl-9-fluorenyl alcohol decreased to 3%; (5) The water bath was removed, and the reaction solution was cooled down to room temperature, and was then transferred to the 20L reactor for post-processing: stirring, standing, and layering; the lower part of the water bath was removed, and the reaction solution was cooled to room temperature. After standing, stratification; the lower aqueous phase was extracted once with 2L of toluene, the organic phases were combined, washed sequentially with 4L of saturated sodium carbonate solution, 4L of water, 4L of saturated saline, and finally the organic phase was dried with 100g of anhydrous magnesium sulfate; (6) after drying for 4 hours, filtration was carried out, and the filter cake was discarded. The filtrate was concentrated to dryness under reduced pressure at 45°C to obtain 1.1kg of white solid with 96% purity by GC; (7) Recrystallization and purification of 9-bromo-9-phenylfluorene: 1.1kg of crude product was added into a 10L reactor, 7L of hexane was added, stirred and heated to reflux, and after the solution became transparent, 50g of activated charcoal was added to decolorize the solution, stirred for 30 minutes, and the filtrate was heat-filtered at 65°C, and the filtrate was naturally The filtrate was cooled to room temperature, then placed in an ice-salt bath and cooled to -5~-10 ℃, and left to stand for 4 hours. Filtering to obtain white crystals, wet weight 1.25 kg. 50 ℃ vacuum drying for 12 hours, to obtain 1.02 kg of yellow crystalline powder, GC purity of 99%, melting point of 99 to 100 ℃, the total yield of 82%.

References

[1] Journal of Organic Chemistry, 2018, vol. 83, # 11, p. 6162 - 6170
[2] Organic Syntheses, 1993, vol. 71, p. 220 - 220
[3] Patent: CN107573208, 2018, A. Location in patent: Paragraph 0022; 0023; 0024; 0025; 0026; 0027; 0028-0032
[4] Patent: CN107337680, 2017, A. Location in patent: Paragraph 0050; 0051; 0054
[5] Patent: CN107573356, 2018, A. Location in patent: Paragraph 0062; 0066; 0067

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