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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2294762Generated: November 1, 2026

4-Toluenesulfonyl chloride → HCID 3296813, compound

https://huagongshe.com/reaction/2294762

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantDiethyl MalonateHCID 7761—
ReactantTriethylamineHCID 8471—
ReactantSodium AzideHCID 33557—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 3296813HCID 329681388.6%

Reaction Steps

A mixture of sodium azide (683 mg, 10.5 mmol), p-toluenesulfonyl chloride (2.0 grams, 10.5 mmol), and 70% aqueous ethanol (30 mL) was stirred at room temperature for 1 hour. Diethyl malonate (1.62 mL, 10.0 mmol) and triethylamine (1.46 mL, 10.5 mmol) were added. The reaction mixture was stirred at room temperature for 1.5 hours and then poured into deionized water (200 mL). The mixture was extracted with petroleum ether. The extracts were combined and decanted from the solid that formed. The petroleum ether solution was washed with a saturated aqueous sodium chloride solution. The organic solution was dried using anhydrous magnesium sulfate, filtered, and concentrated to give 1.65 grams of diethyl 2-diazomalonate as a yellow oil. IR (KBr): 2138, 1757, 1735, 1320, 1092 cm-1. Decomposition temperature: 175° C. (by DSC).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05691098
Source datasetuspto-grants-1997_11
ORD IDord-259ec1b3244a488292360c6ca67d68ba
Source noteuspto-grants-1997_11