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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541163Generated: October 25, 2026

Silane, (chloromethyl)trimethyl- → Bis(diethylamino)(trimethylsilylmethyl)phosphine

https://huagongshe.com/reaction/541163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSilane, (chloromethyl)trimethyl-HCID 75361—
ReactantChlorobis(diethylamino)phosphineHCID 2733351—
ReactantMagnesiumHCID 5462224—
Catalyst1,2-DibromoethaneHCID 7839—
SolventDiethyl EtherHCID 3283—
ProductBis(diethylamino)(trimethylsilylmethyl)phosphineHCID 1504003562%

Reaction Conditions

Temperature-78 °C

Reaction Steps

In a 50 ml three-necked flask equipped with a dropping funnel and a magnetic stirrer, 0.36 g (14.8 mmol) of magnesium and 10 ml of anhydrous diethyl ether were charged at room temperature in a nitrogen gas atmosphere. After several drops of 1,2-dibromoethane were added so as to activate magnesium, 2.0 ml (14.2 mmol) of chloromethyltrimethylsilane were added dropwise carefully to avoid heat build-up. When the reaction solution was stirred for 1 hour while it was heated mildly with a drier, the solution darkened. Then, after the solution was cooled to −78° C., 3.0 g (14.2 mmol) of chlorobis(diethylamino)phosphine synthesized in (a) were added dropwise to the solution, and the resultant mixture was then returned to room temperature and refluxed for 1 hour. The resulting crystals were filtered off, washed with anhydrous diethyl ether, and purified by vacuum-distillation (0.2 kPa, 74.3-79.5° C.) to obtain 2.29 g of bis(diethylamino)(trimethylsilylmethyl)phosphine in the form of a colorless transparent liquid; the yield was 62%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871974B2
Source datasetuspto-grants-2014_10
ORD IDord-3cf6c0ebd9604059b7c62efb57e53d67
Source noteuspto-grants-2014_10