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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1159691Generated: October 26, 2026

Butane → Sec-Butylbenzene

https://huagongshe.com/reaction/1159691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButaneHCID 7843—
Reactant1,3-ButadieneHCID 7845—
ReactantIsobutyleneHCID 8255—
Reactanttrans-2-BUTENEHCID 62695—
Reactantcis-2-BUTENEHCID 5287573—
SolventBenzeneHCID 241—
ProductSec-ButylbenzeneHCID 8680—

Reaction Steps

A 1.0 gram sample of an MCM-22 catalyst (65 wt % MCM-22/35% alumina binder) was used for the alkylation of benzene with Raffinate-2 type feed. This is the same catalyst used in Example 1. The Raffinate-2 type feed is a synthetic blend with the following composition: 53.4% cis-butene, 41.2% trans-butene, 4.6% isobutene, 0.5% butadiene, 0.1% n-butane and 0.2% others. The catalyst was in the form of a 1.6 mm ( 1/16″) diameter cylindrical extrudate and was diluted with sand to 3 cc and loaded into an isothermal, down-flow, fixed-bed, tubular reactor having an outside diameter of 4.76 mm ( 3/16″). The catalyst was dried at 150° C. and 1 atm with 100 cc/min flowing nitrogen for 2 hours. The nitrogen was turned off and benzene was fed to the reactor at 60 cc/hr until reactor pressure reached the desired 300 psig (2170 kPa). Benzene flow was then reduced to 7.63 cc/hr (6.67 WHSV) and Raffinate-2 type feed was introduced from a syringe pump at 2.57 cc/hr (1.6 WHSV). The reactor temperature was adjusted to 160° C. Feed benzene/butene molar ratio was maintained at 3:1 for the entire run. Liquid product was collected in a cold-trap and analyzed off line. Butene conversion was determined by measuring unreacted butene relative to feed butene. The catalyst was on stream for 6 days at 1.6 WHSV of butene with 98% 2-butene conversion, 1 day at 4.8 WHSV with 80% conversion, 1 day at 7.2 WHSV with 62% conversion, and followed by 4 days again at 1.6 WHSV with 97% conversion. Representative data are shown in Table 3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812196B2
Source datasetuspto-grants-2010_10
ORD IDord-4915007964384c949653b1a82636f93d
Source noteuspto-grants-2010_10