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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 377061Generated: November 1, 2026

Fluorobenzene → HCID 19360812, compound

https://huagongshe.com/reaction/377061

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFluorobenzeneHCID 10008—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantTrichloro(2,3-dichloropropyl)silaneHCID 19360815—
ProductHCID 19360812HCID 1936081241%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06022987
Source datasetuspto-grants-2000_02
ORD IDord-1388c80601624ea082e75cff451879fa
Source noteuspto-grants-2000_02