HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982536Generated: October 31, 2026
Hydrochloric Acid → 1,1,2,2-Tetrachloro-1,2-di(propan-2-yl)disilane
https://huagongshe.com/reaction/982536
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Disilane | HCID 74123 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | HCID 14908225 | HCID 14908225 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 1,1,2,2-Tetrachloro-1,2-di(propan-2-yl)disilane | HCID 13837013 | 86% |
Reaction Steps
A 500 ml three necked flask was charged with 300 ml of dry benzene and 48.5 g (0.11 mole) of 1,2-diisopropyl-1,1,2,2-tetraphenyldisilane, and the disilane was uniformly dissolved. To the solution was added 1.5 g of anhydrous aluminium chloride While a dry hydrogen chloride gas was introduced into the benzene solution through a needle tube, the flask was heated for a short time to initiate the reaction. After the reaction once began, generation of heat continued for about 20 minutes After the termination of the exothermic reaction, the introduction of the hydrogen chloride gas was stopped. After 2 ml of dry acetone was added in order to inactivate the aluminium chloride, the solvent was distilled away from the reaction mixture. The residue was subjected to a fractional distillation to give 27 g (0.095 mole, 86% yield) of 1,2-diisopropyl-1,1,2,2-tetrachlorodisilane in a colorless clear liquid (b.p. 55° to 57° C./0.45 Torr).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04996341 |
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| Source dataset | uspto-grants-1991_02 |
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| ORD ID | ord-543f32bb884049e1a1f32f8136800aa2 |
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| Source note | uspto-grants-1991_02 |
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