Cumene → HCID 131728384, compound

HRID 1640082Notes

Reaction equation

HRID 1640082 reaction equation
[C:1]1([CH:7]([CH3:9])[CH3:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:10]=[CH:11][CH3:12]>C1C=CC=CC=1>[CH:7]([C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[CH:11]([CH3:12])[CH3:10])([CH3:9])[CH3:8].[CH:7]([C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1)([CH3:9])[CH3:8]

Participants

4

Procedure

In these experiments, cumene was manufactured by contacting 5.55 parts by weight benzene and 1 part by weight propylene in the batch slurry reactor using the procedure detailed above for Test Sequence for Cumene Manufacture in a Batch Test over catalyst comprising the 0.127 cm MCM-49 quadrulobal catalyst (Material 1) and the 250 to 297 micron catalyst prepared from it by crushing and sieving (Material 2). Cumene (isopropylbenzene, IPB) and diisopropylbenzene (DIPB) products were collected from each experiment and it was found that Material 2 again provided a 30% reduction in the DIPB/IPB ratio.

Workup

  1. customby crushing
  2. filtrationsieving (Material 2)
  3. customCumene (isopropylbenzene, IPB) and diisopropylbenzene (DIPB) products were collected from each experiment and it

Sources & evidence

ORD record
ord-6a2fe08fa94d4158968df7b9e83292e8
Source dataset
uspto-grants-2012_02
Patent number
US08110715B2

Reaction notes

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