Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27876Generated: October 25, 2026

Toluene → 4-(2-Thienylmethyl)-2,2,6,6-tetra-methyl-1-oxa-4-aza-2,6-disilacyclohexane

https://huagongshe.com/reaction/27876

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantTriethylamineHCID 8471—
Reactant(2-Thienylmethyl)amineHCID 34005—
Reactant1,3-Bis(chloromethyl)-1,1,3,3-tetramethyldisiloxaneHCID 75385—
SolventWaterHCID 962—
Product4-(2-Thienylmethyl)-2,2,6,6-tetra-methyl-1-oxa-4-aza-2,6-disilacyclohexaneHCID 23340295—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution containing 22.6 g. (0.2 mole) of 2-thenylamine, 44.4 g. (0.44 mole) of triethylamine and 50.0 g. of acetonitrile dried over molecular sieves there is added 46.2 g. (0.2 mole) of 1,3-bis-chloromethyl-1,1,3,3-tetramethyl-disiloxane. The resulting homogenized solution is allowed to stand for 3 days and then heated in a bath at 90° C. for 36 hours. After cooling the mixture is then equiliberated between toluene and water, the organic phase is then washed with two more portions of water and concentrated to give 61.5 g. of a crude oil. Vacuum distillation through a Vigreux column gives 4-(2-thienylmethyl)-2,2,6,6-tetra-methyl-1-oxa-4-aza-2,6-disilacyclohexane; b.p. 78° to 80° C. at 0.1 to 0.11 mm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04224317
Source datasetuspto-grants-1980_09
ORD IDord-daa0191ef4ad4921942a85e01f0b9bb3
Source noteuspto-grants-1980_09