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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733688Generated: October 30, 2026

Benzene → HCID 20300005, compound

https://huagongshe.com/reaction/1733688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 16765163HCID 16765163—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 20300005HCID 2030000579%

Reaction Steps

To benzene (14 ml) are added 1-hydroxy-4-chloro-1,2,3-benzotriazole (3.4 g) and further triethylamine (2.8 ml). To the solution is added methanesulfonyl chloride (2.3 g) with stirring under ice-cooling and the mixture is stirred at the same temperature for 20 minutes and further at room temperature for 1.5 hours. After allowing to stand overnight, to the reaction mixture are added water (20 ml) and ethyl acetate (30 ml) and the ethyl acetate layer is separated. The water layer is again extracted with ethyl acetate (20 ml). The ethyl acetate extracts are combined, washed with a small amount of a saturated aqueous sodium hydrogen carbonate and water in order, dried over anhydrous sodium sulfate and the solvent is distilled off under a reduced pressure. The residue is washed with petroleum ether (10 ml) to give faint yellow crystals of 1-methanesulfonyloxy-4-chloro-1,2,3-benzotriazole (3.89 g; 79%), melting point: 71°-74° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04242507
Source datasetuspto-grants-1980_12
ORD IDord-7ed8b64cc68340c59fb1663f08d33f05
Source noteuspto-grants-1980_12