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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1678929Generated: October 26, 2026

Pyridine → Tetradec-7-ene

https://huagongshe.com/reaction/1678929

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTetrabutyltinHCID 15098—
ReactantTetradec-7-eneHCID 25209—
ReactantCID 521661HCID 521661—
CatalystTungsten hexachlorideHCID 83301—
ProductTetradec-7-eneHCID 25209—
ProductHexadec-7-eneHCID 520743—
ProductCID 521661HCID 521661—

Reaction Steps

7-Tetradecene and 9-octadecene were cross-metathesized employing a homogeneous modified catalyst. For the reaction, 1 mole 7-tetradecene and 1 mole 9-octadecene were combined in the reactor with 12.9 millimoles tungsten hexachloride. Pyridine (6.5 millimoles) was charged to the reactor followed by the addition of 12.9 millimoles tetrabutyl tin. The reaction was conducted at 90° C and after 30 minutes reaction, near equilibrium conversion of the olefins was obtained with high selectivity to the equilibrium mixture of 1 part 7-tetradecene, 1 part 9-octadecene and 2 parts 7-hexadecene. When the experiment was repeated in an identical manner but using an unmodified catalyst (12.9 millimoles tungsten hexachloride with 12.9 millimoles tetrabutyl tin) conversion of the olefins was significantly greater than the theoretical equilibrium conversion due to the lower selectivity of the reaction to the desired cross-methathesized products.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04078013
Source datasetuspto-grants-1978_03
ORD IDord-7d4b512d0c6a474aaead7ce0c4817963
Source noteuspto-grants-1978_03