HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Dichlorobenzene → [2,2-Bis(2,4-dichlorophenyl)ethyl]trichlorosilane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Dichlorobenzene | HCID 10943 | — |
| Reactant | Silane, trichloro(1,2-dichloroethyl)- | HCID 79093 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | [2,2-Bis(2,4-dichlorophenyl)ethyl]trichlorosilane | HCID 12127967 | 187.2% |
Reaction Steps
In the same apparatus and procedures as EXAMPLE 1 above, 49.1 ml (430 mmol) of 1,3-dichlorobenzene and 2.30 g (17.2 mmol) of aluminum chloride were alkylated with 19.40 g (83.5 mmol) of (1,2-dichloroethyl)trichlorosilane for 30 min at 120° C. The aluminum chloride catalyst was quenched with POCl3 and then stirred for another 1 hour to complete the deactivation. Freshly distilled hexane (100 ml) was added to the reaction mixture and insoluble solids in hexane were filtered from the organic soultion. After hexane was distilled, the reaction products were vacuum distilled to give 14.6 g of [2,2-bis(2,4-dichlorophenyl)ethyl]trichlorosilane (bp; 175-180° C./0.5 torr, yield; 39%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06022987 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-6deb113de3da4c4093a0c08eb6110b20 |
| Source note | uspto-grants-2000_02 |