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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297572Generated: October 29, 2026

Sulfuric Acid → Benzyl-di-t-butylphosphine

https://huagongshe.com/reaction/1297572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantBenzyl ChlorideHCID 7503—
ReactantDi-tert-butylchlorophosphineHCID 139566—
ReactantMagnesiumHCID 5462224—
CatalystCopper bromide (CuBr2)HCID 24611—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductBenzyl-di-t-butylphosphineHCID 1117039489.7%

Reaction Steps

In a 200 ml four-necked flask thoroughly purged with nitrogen, a Grignard reagent solution previously prepared from 8.2 g (0.065 mol) of benzyl chloride and 2.1 g (0.085 mol) of metallic magnesium in 50 ml of tetrahydrofuran, and 0.055 g (0.0003 mol (corresponding to 0.6% by mol)) of copper(II) bromide were placed. To the contents of the flask, 9.0 g (0.05 mol) of di-tert-butylphosphinous chloride was dropwise added as it is without being dissolved in a solvent, over a period of 1 hour at a temperature in the vicinity of 40° C. After the dropwise addition was completed, stirring was conducted at a temperature of 40° C. to 45° C. for 3 hours. After the temperature of the reaction solution was returned to room temperature, 20 ml of toluene and 20 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 was distilled off under reduced pressure, followed by further distillation. Then, fractions given by distillation at 145° C. to 150° C. under reduced pressure of 0.5 Torr were collected. As a result, 10.6 g (purity: 98.5%) of the aimed di-tert-butylbenzylphosphine was obtained as an oily substance. The yield was 88.3%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07250535B2
Source datasetuspto-grants-2007_07
ORD IDord-e7e0005408464992a6686289334aeff5
Source noteuspto-grants-2007_07