HuagongsheHuagongshe Chemistry Print Report · For research reference only
Fluorobenzene → HCID 19360812, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Fluorobenzene | HCID 10008 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | Trichloro(2,3-dichloropropyl)silane | HCID 19360815 | — |
| Product | HCID 19360812 | HCID 19360812 | 41% |
Reaction Steps
In the same apparatus and procedures as EXAMPLE 2 above, 18.8 ml (200 mmol) of fluorobenzene and 0.31 g (2.3 mmol) of aluminum chloride were alkylated with 5.61 g (22.8 mmol) of (2,3-dichloropropyl)trichlorosilane for 10 min at 70° C. The aluminum chloride catalyst was quenched with POCl3 and then stirred for another 1 hour to complete the deactivation. Freshly distilled hexane (50 ml) was added to the reaction mixture and insoluble solids in hexane were filtered from the organic soultion. After hexane and fluorobenzene were distilled, the reaction products were vacuum distilled to give 3.39 g of [3,3-bis(fluorophenyl)propyl]trichlorosilane (bp; 121-122° C./0.5 torr, yield; 41%) as a mixutre of isomers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06022987 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-1388c80601624ea082e75cff451879fa |
| Source note | uspto-grants-2000_02 |