HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297563Generated: October 30, 2026
Sulfuric Acid → 2-(Di-tert-butylphosphino)biphenyl
https://huagongshe.com/reaction/1297563
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-Bromobiphenyl | HCID 16329 | — |
| Reactant | Di-tert-butylchlorophosphine | HCID 139566 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Catalyst | copper(I) bromide | HCID 24593 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(Di-tert-butylphosphino)biphenyl | HCID 2734215 | 88.5% |
Reaction Steps
In a 500 ml four-necked flask thoroughly purged with nitrogen, 9.0 g (0.05 mol) of di-tert-butylphosphinous chloride, 0.07 g (0.0005 mol (corresponding to 1% by mol)) of copper(I) bromide and 50 ml of tetrahydrofuran were placed. To the contents of the flask, a Grignard reagent solution previously prepared from 14.0 g (0.060 mol) of 2-bromobiphenyl and 1.7 g (0.072 mol) of metallic magnesium in 100 ml of tetrahydrofuran was dropwise added over a period of 1 hour with maintaining the temperature at 30° C. to 35° C. After the dropwise addition was completed, stirring was conducted at a reflux temperature for 4 hours. After the temperature of the reaction solution was returned to room temperature, disappearance of di-tert-butylphosphinous chloride was confirmed by gas chromatography. Thereafter, 30 ml of toluene and 30 ml of a 5% sulfuric acid aqueous solution were added to the reaction solution to perform liquid separation. Then, the organic layer was washed with water and dried over anhydrous sodium sulfate. The solvent and a low-boiling component were distilled off under reduced pressure to obtain coarse crystals. The coarse crystals were recrystallized from MeOH to obtain 13.2 g (purity: 99.0%) of the aimed di-tert-butyl(2-phenylphenyl)phosphine. The yield was 87.5%. Melting point: 84-85° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07250535B2 |
|---|
| Source dataset | uspto-grants-2007_07 |
|---|
| ORD ID | ord-9c12fd31a60c49809b83af334474ffce |
|---|
| Source note | uspto-grants-2007_07 |
|---|