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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297566Generated: October 26, 2026

Sulfuric Acid → HCID 22925456, compound

https://huagongshe.com/reaction/1297566

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantChlorobenzeneHCID 7964—
ReactantMagnesiumHCID 5462224—
ReactantDi-tert-amylphosphinous chlorideHCID 23032008—
CatalystCopper, bis(2,4-pentanedionato-O,O')-, (SP-4-1)-HCID 5363992—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22925456HCID 2292545695.9%

Reaction Steps

In a 300 ml four-necked flask thoroughly purged with nitrogen, 20 ml of tetrahydrofuran, 10.4 g (0.050 mol) of di-tert-amylphosphinous chloride and 0.13 g (0.0005 mol (corresponding to 1% by mol)) of copper(II) acetylacetonate were placed. To the contents of the flask, a Grignard reagent solution previously prepared from 6.8 g (0.060 mol) of chlorobenzene and 1.9 g (0.080 mol) of metallic magnesium in 45 ml of tetrahydrofuran was dropwise added over a period of 1 hour with maintaining the temperature at 40° C. to 45° 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, gas chromatography analysis was carried out, and as a result, di-tert-amylphosphinous chloride was present in trace amounts. Thereafter, 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 and a low-boiling component were distilled off under reduced pressure to obtain 12.0 g (purity: 94.4%) of the aimed di-tert-amylphenylphosphine as a viscous oily substance. The yield was 90.5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07250535B2
Source datasetuspto-grants-2007_07
ORD IDord-11f85162040a4f4dbb434f16e2807057
Source noteuspto-grants-2007_07