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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2267207Generated: October 30, 2026

Butane → Sec-Butylbenzene

https://huagongshe.com/reaction/2267207

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButaneHCID 7843—
Reactant1-ButeneHCID 7844—
Reactant1,3-ButadieneHCID 7845—
ReactantIsobutyleneHCID 8255—
Reactanttrans-2-BUTENEHCID 62695—
Reactantcis-2-BUTENEHCID 5287573—
SolventBenzeneHCID 241—
ProductSec-ButylbenzeneHCID 8680—

Reaction Steps

A 0.5 gram sample of an MCM-49 catalyst (1.3 mm [ 1/20″] quadrulobe extrudate of 60% MCM-49/40% Versal 200 alumina binder, cut to 1.3 mm [ 1/20″] length) was used for the alkylation of benzene with a mixed butene feed having 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 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 the reactor pressure increased to 300 psig (2170 kPa). Benzene flow was then reduced to 7.63 cc/hr (6.67 WHSV) and the mixed butene feed was introduced from a syringe pump at 2.57 cc/hr. 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 MCM-49 was on stream for 3 days at 3.2 WHSV of butene with 96% conversion, 1 day at 9.6 WHSV with 80-83% conversion, and 3 days at 3.2 WHSV with 95% conversion. Relative activity of MCM-49 based on first-order butene conversion was 1.1. Representative data are shown in Table 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858832B2
Source datasetuspto-grants-2010_12
ORD IDord-44872a983b094b5a90b28d4a988d3ac6
Source noteuspto-grants-2010_12