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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224535Generated: October 29, 2026

4-Toluenesulfonyl chloride → HCID 23331013, compound

https://huagongshe.com/reaction/224535

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantSodium hydrideHCID 24758—
ReactantHCID 1591522HCID 1591522—
SolventTetrahydrofuranHCID 8028—
ProductHCID 23331013HCID 2333101368%

Reaction Steps

4.6 g (0.02 mole) of N-allyl-2,4-dichlorobenzamide was added to 1.2 g (0.024 mole) of 50% sodium hydride in 20 ml of dry tetrahydrofuran. The mixture was stirred at room temperature for 30 minutes to react them. Then, 4.2 g (0.024 mole) of p-toluenesulfonyl chloride was added, and reacted at room temperature for 1 hour. The tetrahydrofuran was distilled off under reduced pressure. After adding cold water to the residual oil, it was extracted with benzene, dried over anhydrous magnesium sulfate, and concentrated to afford an oily substance. It was purified by silica gel chromatography to afford compound No. 42 shown in Table 2 in a yield of 68%. Its refractive index and elemental analysis values are also shown in Table 2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04233061
Source datasetuspto-grants-1980_11
ORD IDord-b0aa6f071b40435aad1db104603f36e1
Source noteuspto-grants-1980_11