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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Silane, (chloromethyl)trimethyl- | HCID 75361 | — |
| Reactant | Chlorobis(diethylamino)phosphine | HCID 2733351 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Catalyst | 1,2-Dibromoethane | HCID 7839 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Bis(diethylamino)(trimethylsilylmethyl)phosphine | HCID 15040035 | 62% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08871974B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-3cf6c0ebd9604059b7c62efb57e53d67 |
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| Source note | uspto-grants-2014_10 |
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