HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2393677Generated: October 30, 2026
1,3,5-Tribromobenzene → 1,3-Dibromo-5-dimesitylborylbenzene
https://huagongshe.com/reaction/2393677
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3,5-Tribromobenzene | HCID 12279 | — |
| Reactant | Dimesitylboron fluoride | HCID 3466040 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 1,3-Dibromo-5-dimesitylborylbenzene | HCID 18787953 | — |
Reaction Steps
6.25 ml (0.01 mol) of 1.6M butyllithium in hexane are added over 5 minutes at -78° C. to a suspension of 3.14 g (0.01 mol) of 1,3,5-tribromobenzene in 50 ml of diethyl ether. The reaction mixture is stirred at -78° C. for 2 hours, during which a yellow-orange suspension is produced. 2.68 g (0.01 mol) of solid dimesitylfluoroborane are added, and the reaction mixure is warmed to room temperature over about one hour. The mixture is then diluted with 50 ml of hexane and cooled to 0° C. The solid produced is filtered, washed several times with cold hexane and then washed with water and, finally, with methanol, until the solid is colourless. Drying gives 3.54 g (0.0073 mol; i.e. 73% of theory) of a white solid (1,3-dibromo-5-dimesitylborylbenzene). Following purification by chromatography (hexane; SiO2) a melting point of 190°-191° C. is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05807905 |
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| Source dataset | uspto-grants-1998_09 |
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| ORD ID | ord-5af1870a8d6e4441a3d3d2ba812426cc |
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| Source note | uspto-grants-1998_09 |
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