HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1482650Generated: October 31, 2026
Sodium Hydroxide → 6-cyano-1-(4-chlorobutyl)-1H-benzotriazole
https://huagongshe.com/reaction/1482650
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Bromo-4-chlorobutane | HCID 81364 | — |
| Reactant | 1H-1,2,3-benzotriazole-5-carbonitrile | HCID 178509537 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-cyano-1-(4-chlorobutyl)-1H-benzotriazole | HCID 118386861 | 74% |
Reaction Steps
6-cyano-benzotriazole (14.4 g, 0.10 mol) is dissolved into 100 ml of 30% wt. sodium hydroxide, 4-chlorobromobutane (34.3 g, 0.20 mol), tetrabutyl ammonium bromide (0.8 g) are added, and mixed for 5 min. The reaction solution is gradually heated to 60° C., stirred for reaction for 2 hours. Then the reaction solution was cooled down to ambient temperature, 100 ml of dichloromethane was added for extraction and liquid separation. To the aqueous phase, 100 of dichloromethane was added for extraction. Organic phases were mixed, washed with 100 ml of saturated saline. Liquid was separated, and organic phase was evaporated to dryness to produce oily product. Oily products were separated and purified by chromatography with neutral Al2O3, and eluted with dichlormethane to produce 17.3 g of 6-cyano-1-(4-chlorobutyl)-1H-benzotriazole, with a yield of 74.0%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09415047B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-ce40e7cc4dbb4474b0af158ba8fe386f |
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| Source note | uspto-grants-2016_08 |
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