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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119989Generated: October 31, 2026

Tert-Butylamine → 1-(Tert-butylamino)-2-(tetramethylcyclopentadienyl)-1,1,2,2-tetramethyldisilane

https://huagongshe.com/reaction/2119989

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-ButylamineHCID 6385—
Reactant1-Chloro-2-(tetramethylcyclopentadienyl)-1,1,2,2-tetramethyldisilaneHCID 131720373—
SolventDiethyl EtherHCID 3283—
Product1-(Tert-butylamino)-2-(tetramethylcyclopentadienyl)-1,1,2,2-tetramethyldisilaneHCID 131720374—

Reaction Steps

To a solution of 3.000 g (11.0 mmol) 1-chloro-2-(tetramethylcyclopentadienyl)-1,1,2,2-tetramethyldisilane in 50 mL ether was added 2.422 g (33.1 mmol) tertbutylamine. Precipitate formed rapidly. The slurry was stirred for several days at room temperature, then was gently heated to drive the reaction to completion. The solvent was removed, the residue was extracted with pentane, the amine hydrochloride was filtered and the pentane was removed under reduced pressure to give the product as a yellow oil. The yield was 3.150 (92.5%). Mass spec: m/e 309. 1H NMR (C6D6) δ 2.75 (s, 1H), 1.95 (s, 6H), 1.82 (s, 6H),1.08 (s, 9H), 0.51 (s, 1H), 0.24 (s, 6H), 0.16 (s, 6H); 13C NMR (C6D6) δ 135.2, 134.4, 55.2, 50.3, 34.1, 14.9 11.6, 3.3, −1.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06686488B2
Source datasetuspto-grants-2004_02
ORD IDord-b33b631f725246a58ef360cdbbd3d410
Source noteuspto-grants-2004_02