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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733702Generated: October 27, 2026

Triethylamine → HCID 20300011, compound

https://huagongshe.com/reaction/1733702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantStyrene-4-sulfonyl chlorideHCID 9855777—
Reactant1-Hydroxy-6-vinyl-1,2,3-benzotriazoleHCID 23364982—
SolventBenzeneHCID 241—
ProductHCID 20300011HCID 2030001144.2%

Reaction Conditions

Temperature10 °C

Reaction Steps

In benzene (200 ml) are dissolved 1-hydroxy-6-vinyl-1,2,3-benzotriazole (31.2 g) and triethylamine (20 g) under stirring and thereto is added dropwise a solution of p-vinylbenzenesulfonyl chloride (39.2 g) in benzene (70 ml) under ice-cooling to 10° C. The mixture is stirred at room temperature for 3.5 hours. The reaction mixture is poured onto ice-water (1 liter) and the mixture is extracted with ethyl acetate (500 ml, three times). The combined extracts are washed with an aqueous sodium hydrogen carbonate and then water, dried over anhydrous magnesium sulfate, treated with charcoal, and then concentrated under a reduced pressure till about 150 ml. To the mixture is added n-hexane and the mixture is allowed to stand at a cooled place. The precipitated crystals are separated by filtration to give 1-(p-vinylbenzenesulfonyloxy)-6-vinyl-1,2,3-benzotriazole (28.0 g), melting point: 85°-87° C. To the filtrate is further added n-hexane and the mixture is allowed to stand at a cooled place to give additionally the desired product (11.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04242507
Source datasetuspto-grants-1980_12
ORD IDord-a5f6413636a24dccba7792f5864a1149
Source noteuspto-grants-1980_12