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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816469Generated: November 1, 2026

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

https://huagongshe.com/reaction/1816469

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) tert-butylamine. 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 numberUS06884857B1
Source datasetuspto-grants-2005_04
ORD IDord-f73a6137e2c34b41811e2bca1bd8745f
Source noteuspto-grants-2005_04