HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 617681Generated: October 25, 2026
Bromobenzene → Borane, phenylbis(2,4,6-trimethylphenyl)-
https://huagongshe.com/reaction/617681
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromobenzene | HCID 7961 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Dimesitylboron fluoride | HCID 3466040 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Borane, phenylbis(2,4,6-trimethylphenyl)- | HCID 12656091 | — |
Reaction Steps
1.1 equivalents of 1.6 M butyllithium in hexane (37.5 ml, 0.066 mol) are added over the course of 15 minutes at -78° C. to a solution of 9.42 g (0.06 mol) of bromobenzene in 80 ml of tetrahydrofuran (THF). The reaction mixture is stirred at this temperature for 3 h. Then 16.1 g (0.06 mol) of solid dimesitylfluoroborane are added, and the mixture is allowed to warm to room temperature and stirred for a further hour. The mixture is poured into 500 ml of water and the resulting suspension is filtered. The product is purified by trituration with boiling methanol, to give 16.9 g (86% of theory) of the product as a white solid with a melting range of 185-187° C. The shifts δ in the 1H NMR, measured in CDCl3 are 7.50 ppm (d,2,J=7 Hz), 7.46 ppm (t,1,J=10 Hz), 7.50 ppm (br t, 2, J=7 Hz), 6.82 ppm (s, 4), 2.30 ppm (s,6) and 2.00 ppm (s,12).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05952152 |
|---|
| Source dataset | uspto-grants-1999_09 |
|---|
| ORD ID | ord-24329c2645c4466d8326b470aaaeb31c |
|---|
| Source note | uspto-grants-1999_09 |
|---|