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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297569Generated: October 30, 2026

Sulfuric Acid → Di-tert-butyl(isopropyl)phosphine

https://huagongshe.com/reaction/1297569

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant2-ChloropropaneHCID 6361—
ReactantDi-tert-butylchlorophosphineHCID 139566—
ReactantMagnesiumHCID 5462224—
CatalystCuprous chlorideHCID 62652—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductDi-tert-butyl(isopropyl)phosphineHCID 54534892.7%

Reaction Steps

In a 300 ml four-necked flask thoroughly purged with nitrogen, 9.0 g (0.05 mol) of di-tert-butylphosphinous chloride, 0.05 g (0.001 mol (corresponding to 1% by mol)) of copper(I) chloride and 30 ml of tetrahydrofuran were placed. To the contents of the flask, a Grignard reagent solution previously prepared from 4.7 g (0.060 mol) of isopropyl chloride and 1.7 g (0.072 mol) of metallic magnesium in 50 ml of tetrahydrofuran was dropwise added over a period of 1 hour with maintaining the temperature at 25° C. to 30° C. After the dropwise addition was completed, stirring was conducted at the same temperature for 3 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, 20 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 8.2 g (purity: 95.0%) of the aimed di-tert-butylisopropylphosphine as an oily substance. The yield was 92.7%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07250535B2
Source datasetuspto-grants-2007_07
ORD IDord-2dfca7eb6c3a4295ab1268c1831ac6f6
Source noteuspto-grants-2007_07